Name

anterior segment anomalies with or without cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the anterior segment anomalies with or without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.

ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.

congenital anomalies; cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital anomalies; cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain small vessel disease with or without ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

antley-bixler syndrome without genital anomalies or disordered steroidogenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the antley-bixler syndrome without genital anomalies or disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

?testicular anomalies with or without congenital heart disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?testicular anomalies with or without congenital heart disease phenotype from the curated OMIM Gene-Disease Associations dataset.

bifid nose with or without anorectal and renal anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the bifid nose with or without anorectal and renal anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Foveal hypoplasia and anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anterior segment mesenchymal dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anterior segment mesenchymal dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anterior segment mesenchymal dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anterior segment mesenchymal dysgenesis from the curated CTD Gene-Disease Associations dataset.

Foveal Hypoplasia and Anterior Segment Dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset.

abnormality of the anterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior segment of eye aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior segment of eye aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior segment dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior segment dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal anterior eye segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior segment mesenchymal dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the anterior segment mesenchymal dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

cataract, pulverulent or cerulean, with or without microcornea Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract, pulverulent or cerulean, with or without microcornea phenotype from the curated OMIM Gene-Disease Associations dataset.

adult i phenotype without cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the adult i phenotype without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

branchiootorenal syndrome 1, with or without cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the branchiootorenal syndrome 1, with or without cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

Anterior polar cataract 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anterior polar cataract 2 from the curated CTD Gene-Disease Associations dataset.

anterior polar cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior subcapsular cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior polar cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior polar cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior cortical cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior cortical cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Anterior hypothalamic nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior hypothalamic nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

abnormal anterior commissure pars anterior morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior commissure pars anterior morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

globus pallidus, internal segment, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, internal segment, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globus pallidus, external segment, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, external segment, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globus pallidus, internal segment, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, internal segment, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globus pallidus, external segment, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, external segment, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Globus pallidus, internal segment Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Globus pallidus, internal segment relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Globus pallidus, external segment Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Globus pallidus, external segment relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

internal segment of globus pallidus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in internal segment of globus pallidus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

external segment of globus pallidus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in external segment of globus pallidus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

photoreceptor outer segment Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor outer segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor inner segment membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor inner segment membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor inner segment Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor inner segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

axon initial segment Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the axon initial segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor outer segment membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor outer segment membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor outer segment membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the photoreceptor outer segment membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

photoreceptor outer segment Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the photoreceptor outer segment cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

photoreceptor inner segment membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the photoreceptor inner segment membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

photoreceptor inner segment Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the photoreceptor inner segment cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

axon initial segment Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the axon initial segment cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

segment Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term segment in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

proximal convoluted tubule segment 2 development Gene Set

From GO Biological Process Annotations

genes participating in the proximal convoluted tubule segment 2 development biological process from the curated GO Biological Process Annotations dataset.

metanephric proximal convoluted tubule segment 2 development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric proximal convoluted tubule segment 2 development biological process from the curated GO Biological Process Annotations dataset.

photoreceptor cell outer segment organization Gene Set

From GO Biological Process Annotations

genes participating in the photoreceptor cell outer segment organization biological process from the curated GO Biological Process Annotations dataset.

protein localization to photoreceptor outer segment Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to photoreceptor outer segment biological process from the curated GO Biological Process Annotations dataset.

segment specification Gene Set

From GO Biological Process Annotations

genes participating in the segment specification biological process from the curated GO Biological Process Annotations dataset.

photoreceptor outer segment membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor outer segment membrane cellular component from the curated GO Cellular Component Annotations dataset.

photoreceptor outer segment Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor outer segment cellular component from the curated GO Cellular Component Annotations dataset.

photoreceptor inner segment membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor inner segment membrane cellular component from the curated GO Cellular Component Annotations dataset.

photoreceptor inner segment Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor inner segment cellular component from the curated GO Cellular Component Annotations dataset.

axon initial segment Gene Set

From GO Cellular Component Annotations

proteins localized to the axon initial segment cellular component from the curated GO Cellular Component Annotations dataset.

PR segment Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the PR segment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of the posterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

increased upper to lower segment ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the increased upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal st segment Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long-segment aganglionic megacolon Gene Set

From HPO Gene-Disease Associations

genes associated with the long-segment aganglionic megacolon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal upper to lower segment ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

st segment elevation Gene Set

From HPO Gene-Disease Associations

genes associated with the st segment elevation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the posterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the posterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Misato Segment II tubulin-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Misato Segment II tubulin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sperm equatorial segment protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sperm equatorial segment protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

disorganized photoreceptor inner segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short photoreceptor inner segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

photoreceptor inner segment degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the photoreceptor inner segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal photoreceptor outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal photoreceptor outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal st segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal st segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent photoreceptor inner segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal loop of henle ascending limb thick segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal loop of henle ascending limb thick segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

photoreceptor outer segment degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the photoreceptor outer segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal axon initial segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal axon initial segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal photoreceptor inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal photoreceptor inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal posterior eye segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

prolonged st segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the prolonged st segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Heterotrimeric G-protein signaling pathway-rod outer segment phototransduction Gene Set

From PANTHER Pathways

proteins participating in the Heterotrimeric G-protein signaling pathway-rod outer segment phototransduction pathway from the PANTHER Pathways dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sacral agenesis with vertebral anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sacral agenesis with vertebral anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth hormone deficiency with pituitary anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth hormone deficiency with pituitary anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Saethre-Chotzen syndrome with eyelid anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Saethre-Chotzen syndrome with eyelid anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis and dental anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anophthalmos with limb anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anophthalmos with limb anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency-centromeric instability-facial anomalies syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency-centromeric instability-facial anomalies syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Craniosynostosis, anal anomalies, and porokeratosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.

Chondrodysplasia, acromesomelic, with genital anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chondrodysplasia, acromesomelic, with genital anomalies from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Saethre-Chotzen Syndrome with Eyelid Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Saethre-Chotzen Syndrome with Eyelid Anomalies from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.

Cavitary Optic Disc Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cavitary Optic Disc Anomalies from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, associated with Chromosome 5p Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, associated with Chromosome 5p Anomalies from the curated CTD Gene-Disease Associations dataset.

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset.

Coronary Vessel Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Vessel Anomalies from the curated CTD Gene-Disease Associations dataset.

Microcephaly with Mental Retardation and Digital Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly with Mental Retardation and Digital Anomalies from the curated CTD Gene-Disease Associations dataset.

cardiomyopathy; heart anomalies, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy; heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary vessel anomalies; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary vessel anomalies; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pituitary anomalies and holoprosencephaly-like features. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pituitary anomalies and holoprosencephaly-like features. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital anomalies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital anomalies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital anomalies; renal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital anomalies; renal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital; pulmonary hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital; pulmonary hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anomalies Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term anomalies in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

pigmentation anomalies of sun-exposed skin Gene Set

From HPO Gene-Disease Associations

genes associated with the pigmentation anomalies of sun-exposed skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple skeletal anomalies Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple skeletal anomalies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Coronary Vessel Anomalies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Coronary Vessel Anomalies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

chrondrodysplasia, acromesomelic, with genital anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the chrondrodysplasia, acromesomelic, with genital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

robin sequence with cleft mandible and limb anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the robin sequence with cleft mandible and limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

rieger or axenfeld anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the rieger or axenfeld anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency-centromeric instability-facial anomalies syndrome-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency-centromeric instability-facial anomalies syndrome-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

{congenital anomalies of kidney and urinary tract, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {congenital anomalies of kidney and urinary tract, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia with limb anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia with limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

antley-bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the antley-bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

synpolydactyly with foot anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the synpolydactyly with foot anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

saethre-chotzen syndrome with eyelid anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the saethre-chotzen syndrome with eyelid anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

cavitary optic disc anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the cavitary optic disc anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis and dental anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis and dental anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

sacral agenesis with vertebral anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the sacral agenesis with vertebral anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal opacification and other ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal opacification and other ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency-centromeric instability-facial anomalies syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency-centromeric instability-facial anomalies syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

growth hormone deficiency with pituitary anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth hormone deficiency with pituitary anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

cleidocranial dysplasia, forme fruste, dental anomalies only Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleidocranial dysplasia, forme fruste, dental anomalies only phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) pathway from the Reactome Pathways dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, posterior polar, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, posterior polar, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Zonular pulverulent cataract 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Zonular pulverulent cataract 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract 15, multiple types Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract 15, multiple types phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, autosomal dominant, multiple types, with microcornea Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, nuclear total Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, nuclear total phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperferritinemia cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperferritinemia cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Absent corpus callosum cataract immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Absent corpus callosum cataract immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, autosomal recessive congenital 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, zonular Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, zonular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract and cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract and cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, microphthalmia and nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, microphthalmia and nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, membranous Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, membranous phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, juvenile, with microcornea and glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, juvenile, with microcornea and glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital nuclear, autosomal recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital nuclear, autosomal recessive 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Posterior polar cataract type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Posterior polar cataract type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia, high, with cataract and vitreoretinal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract congenital Volkmann type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.

Cataract, Nuclear Progressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Nuclear Progressive from the curated CTD Gene-Disease Associations dataset.

Cataract, Central Saccular, With Sutural Opacities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Central Saccular, With Sutural Opacities from the curated CTD Gene-Disease Associations dataset.

Cataract, posterior polar, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, posterior polar, 4 from the curated CTD Gene-Disease Associations dataset.

Cataract, posterior polar, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, posterior polar, 3 from the curated CTD Gene-Disease Associations dataset.

Cerulean cataract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerulean cataract from the curated CTD Gene-Disease Associations dataset.

Cataract, Zonular Pulverulent 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Zonular Pulverulent 3 from the curated CTD Gene-Disease Associations dataset.

Cataract, Zonular Pulverulent 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Zonular Pulverulent 1 from the curated CTD Gene-Disease Associations dataset.

Hyperferritinemia, hereditary, with congenital cataracts Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset.

Cataract, Juvenile, With Microcornea And Glucosuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Juvenile, With Microcornea And Glucosuria from the curated CTD Gene-Disease Associations dataset.

Absent corpus callosum cataract immunodeficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Absent corpus callosum cataract immunodeficiency from the curated CTD Gene-Disease Associations dataset.

CATARACT 32, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 32, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Zonular, with Sutural Opacities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Zonular, with Sutural Opacities from the curated CTD Gene-Disease Associations dataset.

CATARACT 6, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 6, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Cataract and cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract and cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

Cataract, Age-Related Cortical, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Age-Related Cortical, 1 from the curated CTD Gene-Disease Associations dataset.

Cataract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.

Optic atrophy and cataract, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Recessive Congenital 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Recessive Congenital 3 from the curated CTD Gene-Disease Associations dataset.

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Recessive, Early-Onset, Pulverulent Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Recessive, Early-Onset, Pulverulent from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Dominant, Multiple Types 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Dominant, Multiple Types 1 from the curated CTD Gene-Disease Associations dataset.

Cataract microcornea syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract microcornea syndrome from the curated CTD Gene-Disease Associations dataset.

Cataract, Cortical, Juvenile-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Cortical, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.

Cataract, zonular Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, zonular from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, Autosomal Recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 1 from the curated CTD Gene-Disease Associations dataset.

CATARACT 3, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 3, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Cataract, congenital, with microcornea or slight microphthalmia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, congenital, with microcornea or slight microphthalmia from the curated CTD Gene-Disease Associations dataset.

Cataract, Pulverulent, Juvenile-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Pulverulent, Juvenile-Onset from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated, with Cataract 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 2 from the curated CTD Gene-Disease Associations dataset.

Microphthalmia, Isolated, with Cataract 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microphthalmia, Isolated, with Cataract 1 from the curated CTD Gene-Disease Associations dataset.

HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS from the curated CTD Gene-Disease Associations dataset.

CATARACT 4, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 4, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Cataract, Coppock-Like Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Coppock-Like from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, Autosomal Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.

CATARACT, CONGENITAL OR JUVENILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT, CONGENITAL OR JUVENILE from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, Autosomal Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.

CATARACT 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 23 from the curated CTD Gene-Disease Associations dataset.

cataract Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease cataract from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

senile cataract Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease senile cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

morgagni cataract Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease morgagni cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cataract Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mature cataract Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

immature cataract Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease immature cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

posterior polar cataract Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease posterior polar cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

diabetic cataract Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease diabetic cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital nuclear cataract Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital nuclear cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; exfoliation syndrome; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; exfoliation syndrome; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

zonular pulverulent cataract Gene Set

From GAD Gene-Disease Associations

genes associated with the disease zonular pulverulent cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; exfoliation syndrome; glaucoma; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; exfoliation syndrome; glaucoma; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autosomal dominant coral-like cataract Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autosomal dominant coral-like cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; macular degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract, presenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract, presenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

familial cataract Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; diabetes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; diabetes mellitus type ii; diabetes mellitus, type 2; myopia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital cataracts Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital cataracts in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cataract in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cataractogenesis Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cataractogenesis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cataractassociated Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cataractassociated in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cataractmicrocornea Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cataractmicrocornea in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cataracts Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cataracts in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cataractcausing Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cataractcausing in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Cataracts in type 2 diabetes Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cataracts in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related nuclear cataracts Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related nuclear cataracts phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

cataract Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease cataract in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

cataract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the cataract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

juvenile cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

presenile cataracts Gene Set

From HPO Gene-Disease Associations

genes associated with the presenile cataracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulverulent cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the pulverulent cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior subcapsular cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital nuclear cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sutural cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the sutural cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

iridescent posterior subcapsular cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the iridescent posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior cortical cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

polar cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cortical cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior polar cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

total cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the total cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerulean cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the cerulean cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

punctate cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the punctate cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior y-sutural cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior y-sutural cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

zonular cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the zonular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile cortical cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dense posterior cortical cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the dense posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cortical pulverulent cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the cortical pulverulent cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

membranous cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the membranous cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse nuclear cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subcapsular cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

juvenile zonular cataracts Gene Set

From HPO Gene-Disease Associations

genes associated with the juvenile zonular cataracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nuclear cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lamellar cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the lamellar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Cataract Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cataract phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

nuclear cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the nuclear cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

polar cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the polar cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sutural cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sutural cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lamellar cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lamellar cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

subcapsular cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

posterior subcapsular cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the posterior subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

total cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the total cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cortical cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cortical cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cataract 5, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 5, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 36 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 36 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract, juvenile, with microcornea and glucosuria Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract, juvenile, with microcornea and glucosuria phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 40, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 40, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

hemorrhagic destruction of the brain, subependymal calcification, and cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemorrhagic destruction of the brain, subependymal calcification, and cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 9, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 9, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract with late-onset corneal dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract with late-onset corneal dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

myopia, high, with cataract and vitreoretinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 30, pulverulent Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 30, pulverulent phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 22, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 22, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, cataract, retinitis pigmentosa, and sperm abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, cataract, retinitis pigmentosa, and sperm abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 3, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 3, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataract 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataract 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataract 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataract 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 1, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 1, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

galactokinase deficiency with cataracts Gene Set

From OMIM Gene-Disease Associations

genes associated with the galactokinase deficiency with cataracts phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 29, coralliform Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 29, coralliform phenotype from the curated OMIM Gene-Disease Associations dataset.

{cataract 28, age-related cortical, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {cataract 28, age-related cortical, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 20, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 20, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 33 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 33 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 14, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 14, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 37, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 37, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 12, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 12, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 39, multiple types, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperferritinemia-cataract syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperferritinemia-cataract syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 34, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 34, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital cataracts, hearing loss, and neurodegeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital cataracts, hearing loss, and neurodegeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital cataracts, facial dysmorphism, and neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital cataracts, facial dysmorphism, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 11, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 11, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 6, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 6, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 2, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 2, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 16, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 16, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 15, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 15, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

optic atrophy 3 with cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 11, syndromic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 11, syndromic phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 18, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 18, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataract, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataract, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 17, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 17, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 27, nuclear progressive Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 27, nuclear progressive phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 4, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 4, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 31, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 31, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 10, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 10, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 38, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 38, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia with cataract 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia with cataract 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia with cataract 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia with cataract 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 13 with adult i phenotype Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 13 with adult i phenotype phenotype from the curated OMIM Gene-Disease Associations dataset.

?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 35, congenital nuclear Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 35, congenital nuclear phenotype from the curated OMIM Gene-Disease Associations dataset.

Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bronchiectasis with or without elevated sweat chloride 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, and autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 12 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy, cystic, without megalencephaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy, cystic, without megalencephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cognitive impairment with or without cerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 19 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 17 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bronchiectasis with or without elevated sweat chloride 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, without vestibular involvement, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, without vestibular involvement, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Capillary malformation without arteriovenous malformation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Capillary malformation without arteriovenous malformation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acrodysostosis 2, with or without hormone resistance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acrodysostosis 2, with or without hormone resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 13 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 10 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Focal epilepsy with speech disorder with or without mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypogonadotropic hypogonadism 11 with or without anosmia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IFAP syndrome with or without BRESHECK syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency 26 with or without neurologic abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency 26 with or without neurologic abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

H2AX complex, isolated from cells without IR exposure Gene Set

From CORUM Protein Complexes

proteins in the H2AX complex, isolated from cells without IR exposure protein complex from the CORUM Protein Complexes dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy, Cystic, Without Megalencephaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy, Cystic, Without Megalencephaly from the curated CTD Gene-Disease Associations dataset.

NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Migraine without Aura from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 1 from the curated CTD Gene-Disease Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 2 from the curated CTD Gene-Disease Associations dataset.

Bronchiectasis With Or Without Elevated Sweat Chloride 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bronchiectasis With Or Without Elevated Sweat Chloride 3 from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency without anhidrotic ectodermal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency without anhidrotic ectodermal dysplasia from the curated CTD Gene-Disease Associations dataset.

HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.

EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.

Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.

MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA) from the curated CTD Gene-Disease Associations dataset.

Metaphyseal Dysplasia without Hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metaphyseal Dysplasia without Hypotrichosis from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PULMONARY HYPERTENSION, CHRONIC THROMBOEMBOLIC, WITHOUT DEEP VEIN THROMBOSIS, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA from the curated CTD Gene-Disease Associations dataset.

Nonmedullary thyroid carcinoma, with or without cell oxyphilia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nonmedullary thyroid carcinoma, with or without cell oxyphilia from the curated CTD Gene-Disease Associations dataset.

SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.

Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia from the curated CTD Gene-Disease Associations dataset.

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Migraine without Aura in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

migraine without aura Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease migraine without aura in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cleft lip with cleft palate; cleft lip without cleft palate; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

salmeterol with or without fluticasone propionate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease salmeterol with or without fluticasone propionate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; migraine with aura; migraine without aura; tension-type headache Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; migraine with aura; migraine without aura; tension-type headache in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with or without cleft palate; cleft palate, isolated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with or without cleft palate; cleft palate, isolated in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with cleft palate; cleft lip without cleft palate; cleft lip Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate; cleft lip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv; tuberculosis; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine with aura; migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nonsyndromic cleft lipor without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nonsyndromic cleft lipor without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine with and without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine with and without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip without cleft palate; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip without cleft palate; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

migraine disorders; migraine with aura; migraine without aura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease migraine disorders; migraine with aura; migraine without aura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nonsyndromic cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nonsyndromic cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

without Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term without in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

cell cycle comprising mitosis without cytokinesis Gene Set

From GO Biological Process Annotations

genes participating in the cell cycle comprising mitosis without cytokinesis biological process from the curated GO Biological Process Annotations dataset.

Migraine without aura Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Migraine without aura phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

migraine without aura Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease migraine without aura in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

migraine without aura Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the migraine without aura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

focal seizures without impairment of consciousness or awareness Gene Set

From HPO Gene-Disease Associations

genes associated with the focal seizures without impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

migraine without aura Gene Set

From HPO Gene-Disease Associations

genes associated with the migraine without aura phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Migraine without Aura Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Migraine without Aura phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypogonadotropic hypogonadism 15 with or without anosmia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypogonadotropic hypogonadism 15 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

paragangliomas 1, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the paragangliomas 1, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 4 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 14 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 14 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

waardenburg syndrome, type 2e, with or without neurologic involvement Gene Set

From OMIM Gene-Disease Associations

genes associated with the waardenburg syndrome, type 2e, with or without neurologic involvement phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 2, primary, autosomal recessive, with or without cortical malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

cognitive impairment with or without cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 6 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 10 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 10 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 3 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 3 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine without aura, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine without aura, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 8 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 8 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukemia, megakaryoblastic, with or without down syndrome, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukemia, megakaryoblastic, with or without down syndrome, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 5 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 5 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 7 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

?microtia with or without hearing impairment (ad) Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microtia with or without hearing impairment (ad) phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, x-linked, with/without neutropenia and/or platelet abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, x-linked, with/without neutropenia and/or platelet abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 11 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 11 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 18 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 18 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

{bronchiectasis with or without elevated sweat chloride 1, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bronchiectasis with or without elevated sweat chloride 1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, with or without aura, susceptibility to, 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, with or without aura, susceptibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema Gene Set

From OMIM Gene-Disease Associations

genes associated with the dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 2 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 2 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

bronchiectasis with or without elevated sweat chloride 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bronchiectasis with or without elevated sweat chloride 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 6, autosomal recessive, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

acrodysostosis 1, with or without hormone resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the acrodysostosis 1, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 20 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 20 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

?hypogonadotropic hypogonadism 13 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hypogonadotropic hypogonadism 13 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

pulmonary hypertension, familial primary, 1, with or without hht Gene Set

From OMIM Gene-Disease Associations

genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset.

?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 1, with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 4 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 4 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

dementia, frontotemporal, with or without parkinsonism Gene Set

From OMIM Gene-Disease Associations

genes associated with the dementia, frontotemporal, with or without parkinsonism phenotype from the curated OMIM Gene-Disease Associations dataset.

leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 9 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 9 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 9 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine without aura, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine without aura, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 1, with or without congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 1, with or without congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

tooth agenesis, selective, 1, with or without orofacial cleft Gene Set

From OMIM Gene-Disease Associations

genes associated with the tooth agenesis, selective, 1, with or without orofacial cleft phenotype from the curated OMIM Gene-Disease Associations dataset.

{pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

?hypogonadotropic hypogonadism 12 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hypogonadotropic hypogonadism 12 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 6 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 6 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 9, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 9, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombocytopenia, x-linked, with or without dyserythropoietic anemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombocytopenia, x-linked, with or without dyserythropoietic anemia phenotype from the curated OMIM Gene-Disease Associations dataset.

gastric cancer, familial diffuse, with or without cleft lip and/or palate Gene Set

From OMIM Gene-Disease Associations

genes associated with the gastric cancer, familial diffuse, with or without cleft lip and/or palate phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, progressive myoclonic 4, with or without renal failure Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 1 with or without anosmia (kallmann syndrome 1) phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 7, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 7, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

gyrate atrophy of choroid and retina with or without ornithinemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 19 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 19 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with or without aura, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, with or without nystagmus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, neurosensory, without vestibular involvement, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, neurosensory, without vestibular involvement, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 14, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 14, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy, cystic, without megalencephaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy, cystic, without megalencephaly phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with or without aura, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 8 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

mcleod syndrome with or without chronic granulomatous disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the mcleod syndrome with or without chronic granulomatous disease phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine with or without aura, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine with or without aura, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 1, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 1, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial dna depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) phenotype from the curated OMIM Gene-Disease Associations dataset.

{migraine, with or without aura, susceptibility to, 13} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {migraine, with or without aura, susceptibility to, 13} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypogonadotropic hypogonadism 16 with or without anosmia} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypogonadotropic hypogonadism 16 with or without anosmia} phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

androgen insensitivity, partial, with or without breast cancer Gene Set

From OMIM Gene-Disease Associations

genes associated with the androgen insensitivity, partial, with or without breast cancer phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 17 with or without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 17 with or without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, focal, with speech disorder and with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

encephalopathy, progressive, with or without lipodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 2 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, autosomal recessive 2 with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, autosomal recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

ifap syndrome with or without bresheck syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertrichosis terminalis, generalized, with or without gingival hyperplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertrichosis terminalis, generalized, with or without gingival hyperplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 16, with or without neurologic abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 16, with or without neurologic abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 5 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine with or without aura, susceptibility to Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine with or without aura, susceptibility to phenotype from the curated OMIM Gene-Disease Associations dataset.

ciliary dyskinesia, primary, 3, with or without situs inversus Gene Set

From OMIM Gene-Disease Associations

genes associated with the ciliary dyskinesia, primary, 3, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

acrodysostosis 2, with or without hormone resistance Gene Set

From OMIM Gene-Disease Associations

genes associated with the acrodysostosis 2, with or without hormone resistance phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperproinsulinemia, familial, with or without diabetes Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperproinsulinemia, familial, with or without diabetes phenotype from the curated OMIM Gene-Disease Associations dataset.

left ventricular noncompaction 3, with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the left ventricular noncompaction 3, with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

hypogonadotropic hypogonadism 7 without anosmia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypogonadotropic hypogonadism 7 without anosmia phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

nephrotic syndrome, type 5, with or without ocular abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the nephrotic syndrome, type 5, with or without ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.

sweat chloride elevation without cf Gene Set

From OMIM Gene-Disease Associations

genes associated with the sweat chloride elevation without cf phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 15, with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 15, with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

?cardiac conduction disease with or without dilated cardiomyopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cardiac conduction disease with or without dilated cardiomyopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 10, with or without ftd Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 10, with or without ftd phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, multinodular 1, with or without sertoli-leydig cell tumors Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, multinodular 1, with or without sertoli-leydig cell tumors phenotype from the curated OMIM Gene-Disease Associations dataset.

anterior group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior orbital gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior orbital gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, anterior region, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, left, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior group of nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, anterior region, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, left, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior hypothalamic area, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior hypothalamic area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior orbital gyrus, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior orbital gyrus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior hypothalamic area, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior hypothalamic area, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior olfactory area, dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior olfactory area, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior olfactory area, ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior olfactory area, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior tegmental nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior tegmental nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, layer 2/3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 5 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

nucleus of the stria terminalis, medial division, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in nucleus of the stria terminalis, medial division, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior paraventricular nucleus of thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior paraventricular nucleus of thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, anterolateral area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, anterolateral area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior pretectal nucleus, ventral core part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior pretectal nucleus, ventral core part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, oval nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, oval nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior nuclei Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior nuclei relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Dorsomedial nucleus of the hypothalamus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Dorsomedial nucleus of the hypothalamus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior digastric muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior digastric muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

interstitial nucleus of the posterior limb of the anterior commissure Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in interstitial nucleus of the posterior limb of the anterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, layer 5 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, fusiform nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, fusiform nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, ventral nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, ventral nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior hypothalamic nucleus, central part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, juxtacapsular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, juxtacapsular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, anteromedial area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, anteromedial area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Basolateral amygdalar nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basolateral amygdalar nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior pretectal nucleus, ventral superficial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior pretectal nucleus, ventral superficial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nucleus of the anterior commissure Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nucleus of the anterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior pretectal nucleus, dorsal superficial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior pretectal nucleus, dorsal superficial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, lateral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior pretectal nucleus, dorsal core part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior pretectal nucleus, dorsal core part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basomedial amygdaloid nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basomedial amygdaloid nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Ventral anterior-lateral complex of the thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Ventral anterior-lateral complex of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior amygdalar area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior amygdalar area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 2/3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, external part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, external part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cortical amygdalar area, anterior part, layer 2 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cortical amygdalar area, anterior part, layer 2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, medial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, rhomboid nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, rhomboid nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basolateral amygdaloid nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basolateral amygdaloid nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior hypothalamic nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cortical amygdalar area, anterior part, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cortical amygdalar area, anterior part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Basomedial amygdalar nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basomedial amygdalar nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, posteroventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, posteroventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior part of Int Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior part of Int relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior hypothalamic nucleus, posterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior hypothalamic nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, 6b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, 6a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, magnocellular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, magnocellular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cortical amygdalar area, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cortical amygdalar area, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior pretectal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior pretectal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 6b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 6a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, dorsomedial nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, dorsomedial nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

posterior part of anterior hypothalamic nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior part of anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral anterior hypothalamic nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Ventromedial hypothalamic nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Ventromedial hypothalamic nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior cortical amygdaloid area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior cortical amygdaloid area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_15 yrs_M_12299 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12960 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_F_12365 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_40 yrs_F_12304 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_4 yrs_M_12298 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_19 yrs_F_12832 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12981 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_11 yrs_F_12289 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_37 pcw_M_263195015 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12890 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior hypothalamic nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

anterior nucleus of pulvinar Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior nucleus of pulvinar relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

anterior cortical nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior cortical nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

ventral anterior nucleus of thalamus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in ventral anterior nucleus of thalamus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

anterior amygdaloid area Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior amygdaloid area relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, anterior part Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior part relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

rostral (anterior) extramural migratory stream Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral (anterior) extramural migratory stream relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal arthrogryposis with anterior horn cell disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.

Sacral defect and anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

Myopathy, Distal, with Anterior Tibial Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.

Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease from the curated CTD Gene-Disease Associations dataset.

anterior spinal artery syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior spinal artery syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior horn cell disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior horn cell disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior compartment syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior compartment syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior cranial fossa meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior cranial fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior uveitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior uveitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior scleritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior scleritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior cerebral artery infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior ischemic optic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

rheumatoid spondylitis; spondylitis, ankylosing; uveitis, anterior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rheumatoid spondylitis; spondylitis, ankylosing; uveitis, anterior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

uveitis, anterior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease uveitis, anterior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute anterior uveitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute anterior uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term anterior in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

H6PD_KO_GDS3195_603_mouse_Skeletal muscle - Tibialis anterior Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the H6PD_KO_GDS3195_603_mouse_Skeletal muscle - Tibialis anterior gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

positive regulation of anterior head development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of anterior head development biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior axis specification, embryo Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations dataset.

specification of ureteric bud anterior/posterior symmetry Gene Set

From GO Biological Process Annotations

genes participating in the specification of ureteric bud anterior/posterior symmetry biological process from the curated GO Biological Process Annotations dataset.

anterior neuropore closure Gene Set

From GO Biological Process Annotations

genes participating in the anterior neuropore closure biological process from the curated GO Biological Process Annotations dataset.

anterior compartment pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the anterior compartment pattern formation biological process from the curated GO Biological Process Annotations dataset.

cardioblast anterior-lateral migration Gene Set

From GO Biological Process Annotations

genes participating in the cardioblast anterior-lateral migration biological process from the curated GO Biological Process Annotations dataset.

negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

anterior commissure morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the anterior commissure morphogenesis biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

polarity specification of anterior/posterior axis Gene Set

From GO Biological Process Annotations

genes participating in the polarity specification of anterior/posterior axis biological process from the curated GO Biological Process Annotations dataset.

specification of anterior mesonephric tubule identity Gene Set

From GO Biological Process Annotations

genes participating in the specification of anterior mesonephric tubule identity biological process from the curated GO Biological Process Annotations dataset.

epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

genes participating in the epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations dataset.

spemann organizer formation at the anterior end of the primitive streak Gene Set

From GO Biological Process Annotations

genes participating in the spemann organizer formation at the anterior end of the primitive streak biological process from the curated GO Biological Process Annotations dataset.

zygotic determination of anterior/posterior axis, embryo Gene Set

From GO Biological Process Annotations

genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations dataset.

regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axis specification biological process from the curated GO Biological Process Annotations dataset.

fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural plate anterior/posterior regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations dataset.

spinal cord anterior/posterior patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axon guidance biological process from the curated GO Biological Process Annotations dataset.

regulation of anterior head development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of anterior head development biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in ureteric bud development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in ureteric bud development biological process from the curated GO Biological Process Annotations dataset.

anterior semicircular canal development Gene Set

From GO Biological Process Annotations

genes participating in the anterior semicircular canal development biological process from the curated GO Biological Process Annotations dataset.

thorax and anterior abdomen determination Gene Set

From GO Biological Process Annotations

genes participating in the thorax and anterior abdomen determination biological process from the curated GO Biological Process Annotations dataset.

regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

forebrain anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the forebrain anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription involved in anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations dataset.

Anterior chamber depth Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Anterior chamber depth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of the anterior pituitary Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

anterior chamber synechiae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior chamber synechiae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

irregular ossification at anterior rib ends Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular ossification at anterior rib ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior beaking of lumbar vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior beaking of lumbar vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior encephalocele Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior encephalocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

left anterior fascicular block Gene Set

From HPO Gene-Disease Associations

genes associated with the left anterior fascicular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior tibial bowing Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior tibial bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior beaking of thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior beaking of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior rib cupping Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior rib cupping phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the small anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

wide anterior fontanel Gene Set

From HPO Gene-Disease Associations

genes associated with the wide anterior fontanel phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thick anterior alveolar ridges Gene Set

From HPO Gene-Disease Associations

genes associated with the thick anterior alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior sacral meningocele Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior sacral meningocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior clefting of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior clefting of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior hypopituitarism Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior hypopituitarism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

deep anterior chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the deep anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior creases of earlobe Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior creases of earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

polymicrogyria, anterior to posterior gradient Gene Set

From HPO Gene-Disease Associations

genes associated with the polymicrogyria, anterior to posterior gradient phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low anterior hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the low anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior open-bite malocclusion Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior open-bite malocclusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the anterior pituitary Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the anterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior open bite Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior open bite phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior basal encephalocele Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior basal encephalocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior beaking of lower thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior beaking of lower thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline skin dimples over anterior/posterior fontanelles Gene Set

From HPO Gene-Disease Associations

genes associated with the midline skin dimples over anterior/posterior fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal anterior horn cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

delayed closure of the anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the delayed closure of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nonarteritic anterior ischemic optic neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the nonarteritic anterior ischemic optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

persistent open anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the persistent open anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior pituitary Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paucity of anterior horn motor neurons Gene Set

From HPO Gene-Disease Associations

genes associated with the paucity of anterior horn motor neurons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior bowing of long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior bowing of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior lenticonus Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior lenticonus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior wedging of l2 Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior wedging of l2 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior wedging of l1 Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior wedging of l1 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior rounding of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior rounding of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disorganization of the anterior cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the disorganization of the anterior cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

shallow anterior chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the shallow anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior pituitary dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior pituitary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high anterior hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the high anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior rib punctate calcifications Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior rib punctate calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior pituitary agenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior pituitary agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior pituitary hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior pituitary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior radial head dislocation Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior radial head dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

degeneration of anterior horn cells Gene Set

From HPO Gene-Disease Associations

genes associated with the degeneration of anterior horn cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior concavity of thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior concavity of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent anterior eye chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the absent anterior eye chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Anterior Wall Myocardial Infarction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anterior Wall Myocardial Infarction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.