Name

inner ear hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

aplasia/hypoplasia of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.

inner ear disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease inner ear disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

inner ear disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

inner ear morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the inner ear morphogenesis biological process from the curated GO Biological Process Annotations dataset.

inner ear receptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of inner ear receptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

inner ear receptor cell development Gene Set

From GO Biological Process Annotations

genes participating in the inner ear receptor cell development biological process from the curated GO Biological Process Annotations dataset.

regulation of inner ear receptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

inner ear development Gene Set

From GO Biological Process Annotations

genes participating in the inner ear development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of inner ear receptor cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations dataset.

inner ear receptor stereocilium organization Gene Set

From GO Biological Process Annotations

genes participating in the inner ear receptor stereocilium organization biological process from the curated GO Biological Process Annotations dataset.

inner ear receptor cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the inner ear receptor cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

inner ear disease Gene Set

From GWASdb SNP-Disease Associations

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

neoplasm of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the vestibule of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

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

dilated vestibule of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the dilated vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

functional abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the functional abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the inner ear Gene Set

From HPO Gene-Disease Associations

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

inner ear cysts Gene Set

From MPO Gene-Phenotype Associations

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

delayed inner ear development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner ear vestibule Gene Set

From MPO Gene-Phenotype Associations

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

abnormal blood-inner ear barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-inner ear barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner ear canal morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner ear canal fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner ear canal fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner ear development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner ear morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner ear vestibule morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent inner ear Gene Set

From MPO Gene-Phenotype Associations

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

deafness, congenital with inner ear agenesis, microtia, and microdontia Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, congenital with inner ear agenesis, microtia, and microdontia phenotype from the curated OMIM Gene-Disease Associations dataset.

inner ear Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue inner ear from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

inner ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner ear vestibulum Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner ear vestibulum in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

aplasia/hypoplasia of the ear Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the ear cartilage Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ear cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the external ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ear lobe hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

Scalp ear nipple syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Scalp ear nipple syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ear Diseases Gene Set

From CTD Gene-Disease Associations

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

Ear, External Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Ear, External in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

cholesteatoma of middle ear Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

external ear cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

external ear disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

middle ear squamous cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease middle ear squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

middle ear cholesteatoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

middle ear carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

middle ear adenoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

external ear carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

middle ear cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

middle ear disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

ear Gene Set

From GeneRIF Biological Term Annotations

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

ear development Gene Set

From GO Biological Process Annotations

genes participating in the ear development biological process from the curated GO Biological Process Annotations dataset.

ear morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the ear morphogenesis biological process from the curated GO Biological Process Annotations dataset.

middle ear morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the middle ear morphogenesis biological process from the curated GO Biological Process Annotations dataset.

outer ear morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the outer ear morphogenesis biological process from the curated GO Biological Process Annotations dataset.

middle ear disease Gene Set

From GWASdb SNP-Disease Associations

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

morphological abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ear Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the middle ear ossicles Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

stahl ear Gene Set

From HPO Gene-Disease Associations

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

round ear Gene Set

From HPO Gene-Disease Associations

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

crumpled ear Gene Set

From HPO Gene-Disease Associations

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

external ear malformation Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ear Gene Set

From HPO Gene-Disease Associations

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

protruding ear Gene Set

From HPO Gene-Disease Associations

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

cupped ear Gene Set

From HPO Gene-Disease Associations

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

neoplasm of the outer ear Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the outer ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

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

fusion of middle ear ossicles Gene Set

From HPO Gene-Disease Associations

genes associated with the fusion of middle ear ossicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lop ear Gene Set

From HPO Gene-Disease Associations

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

abnormal middle ear reflexes Gene Set

From HPO Gene-Disease Associations

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

functional abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the functional abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of the outer ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of the middle ear ossicles Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle ear ossicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short ear Gene Set

From HPO Gene-Disease Associations

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

long ear Gene Set

From HPO Gene-Disease Associations

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

Ear Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Adaptin ear-binding coat-associated protein 1 NECAP-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adaptin ear-binding coat-associated protein 1 NECAP-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EAR Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EAR protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal ear development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear distance/ position Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

lowered ear position Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal outer ear morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal middle ear morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal middle ear morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent middle ear ossicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent middle ear ossicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal middle ear ossicle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal middle ear ossicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hearing/vestibular/ear phenotype Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hearing/vestibular/ear phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ear shape Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear morphology Gene Set

From MPO Gene-Phenotype Associations

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

delayed ear emergence Gene Set

From MPO Gene-Phenotype Associations

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

absent outer ear Gene Set

From MPO Gene-Phenotype Associations

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

decreased ear pigmentation Gene Set

From MPO Gene-Phenotype Associations

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

fusion of middle ear ossicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fusion of middle ear ossicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ear lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ear lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ear telangiectases Gene Set

From MPO Gene-Phenotype Associations

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

ear inflammation Gene Set

From MPO Gene-Phenotype Associations

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

scalp-ear-nipple syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the scalp-ear-nipple syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

ear Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue ear from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

ear Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue ear in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

corn ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue corn ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

middle ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue middle ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

outer ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue outer ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

ear Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue ear in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

OB inner plexiform layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in OB inner plexiform layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Main olfactory bulb, inner plexiform layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Main olfactory bulb, inner plexiform layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

inner SZ in posterior parahippocampal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in rostral perirhinal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in rostral perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in orbital frontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in orbital frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in inferolateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner portion of medial ganglionic eminence Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner portion of medial ganglionic eminence relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in medial temporal-occipital cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in dorsomedial frontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in dorsomedial frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in (rostral) midinferior temporal cortex (area 36) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in (rostral) midinferior temporal cortex (area 36) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in lateral temporal-occipital cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in dorsolateral prefrontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in dorsolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in midinferior temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in midinferior temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in primary visual cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in caudal cingulate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in ventrolateral prefrontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in ventrolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in granular insular cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in granular insular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in primary auditory cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in dorsomedial frontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in dorsomedial frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in inferolateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in inferolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in caudal midinferior temporal cortex (area TF) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in ventromedial extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in ventromedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in posterior parahippocampal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in caudal perirhinal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in caudal midinferior temporal cortex (area TF) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in ventromedial extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in ventromedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in midcingulate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in midcingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in posteroinferior (ventral) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in posteroinferior (ventral) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in midlateral extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in midlateral extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in primary somatosensory cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in posterosuperior (dorsal) parietal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in posterosuperior (dorsal) parietal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in lateral temporal-occipital cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in lateral temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in ventrolateral prefrontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in ventrolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in primary somatosensory cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in midlateral extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in midlateral extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in superolateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in dorsomedial parietal cortex (area 7m) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in dorsomedial parietal cortex (area 7m) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in dorsomedial extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in dorsomedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in subgenual (subcallosal) cingulate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in subgenual (subcallosal) cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in frontal polar cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in frontal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in dysgranular insular cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in dysgranular insular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in dorsomedial extrastriate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in dorsomedial extrastriate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in medial temporal-occipital cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in medial temporal-occipital cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in temporal polar cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in temporal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in midlateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in midlateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner CP in rostral cingulate cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner CP in rostral cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in frontal polar cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in frontal polar cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in dorsolateral prefrontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in dorsolateral prefrontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner portion of lateral ganglionic eminence Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner portion of lateral ganglionic eminence relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in orbital frontal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in orbital frontal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in superolateral temporal cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in superolateral temporal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in primary visual cortex Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

inner SZ in posteror frontal cortex (motor cortex) Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in inner SZ in posteror frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

condensed chromosome inner kinetochore Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed chromosome inner kinetochore cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial inner membrane peptidase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

organelle inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

inner acrosomal membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

intrinsic component of nuclear inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of nuclear inner membrane 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.

mitochondrial inner membrane presequence translocase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial inner membrane presequence translocase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intrinsic component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

integral component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of mitochondrial inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extrinsic component of mitochondrial inner 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.

mitochondrial inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

integral component of nuclear inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the integral component of nuclear inner membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

inner mucus layer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

nuclear inner membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

plastid inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

condensed chromosome inner kinetochore Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

inner dynein arm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

mitochondrial inner membrane peptidase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

viral inner capsid Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

female germline ring canal inner rim Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the female germline ring canal inner rim cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

inner acrosomal membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

organelle inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the organelle inner membrane 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.

mitochondrial inner membrane presequence translocase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

intrinsic component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

integral component of mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the integral component of mitochondrial inner 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.

mitochondrial inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

inner mucus layer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

chloroplast inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

inner membrane complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

mitochondrial inner membrane protein insertion complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

nuclear inner membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

inner Gene Set

From GeneRIF Biological Term Annotations

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

nuclear inner membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the nuclear inner membrane organization biological process from the curated GO Biological Process Annotations dataset.

inner cell mass cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the inner cell mass cell differentiation biological process from the curated GO Biological Process Annotations dataset.

renal inner medulla development Gene Set

From GO Biological Process Annotations

genes participating in the renal inner medulla development biological process from the curated GO Biological Process Annotations dataset.

inner cell mass cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the inner cell mass cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

inner medullary collecting duct development Gene Set

From GO Biological Process Annotations

genes participating in the inner medullary collecting duct development biological process from the curated GO Biological Process Annotations dataset.

protein import into mitochondrial inner membrane Gene Set

From GO Biological Process Annotations

genes participating in the protein import into mitochondrial inner membrane biological process from the curated GO Biological Process Annotations dataset.

inner cell mass cellular morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the inner cell mass cellular morphogenesis biological process from the curated GO Biological Process Annotations dataset.

inner dynein arm assembly Gene Set

From GO Biological Process Annotations

genes participating in the inner dynein arm assembly biological process from the curated GO Biological Process Annotations dataset.

inner cell mass cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the inner cell mass cell proliferation biological process from the curated GO Biological Process Annotations dataset.

inner mitochondrial membrane organization Gene Set

From GO Biological Process Annotations

genes participating in the inner mitochondrial membrane organization biological process from the curated GO Biological Process Annotations dataset.

condensed chromosome inner kinetochore Gene Set

From GO Cellular Component Annotations

proteins localized to the condensed chromosome inner kinetochore cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane peptidase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial inner membrane peptidase complex cellular component from the curated GO Cellular Component Annotations dataset.

organelle inner membrane Gene Set

From GO Cellular Component Annotations

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

inner acrosomal membrane Gene Set

From GO Cellular Component Annotations

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

intrinsic component of nuclear inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of nuclear inner membrane 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.

integral component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane presequence translocase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial inner membrane presequence translocase complex cellular component from the curated GO Cellular Component Annotations dataset.

extrinsic component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the extrinsic component of mitochondrial inner 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.

intrinsic component of mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the intrinsic component of mitochondrial inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial inner membrane Gene Set

From GO Cellular Component Annotations

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

integral component of nuclear inner membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the integral component of nuclear inner membrane cellular component from the curated GO Cellular Component Annotations dataset.

inner mucus layer Gene Set

From GO Cellular Component Annotations

proteins localized to the inner mucus layer cellular component from the curated GO Cellular Component Annotations dataset.

nuclear inner membrane Gene Set

From GO Cellular Component Annotations

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

absent inner and outer dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent inner and outer dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent inner dynein arms Gene Set

From HPO Gene-Disease Associations

genes associated with the absent inner dynein arms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Mitochondrial import inner membrane translocase subunit Tim21 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim21 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim44 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim44 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim10/Tim12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim10/Tim12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Inner centromere protein, ARK-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Inner centromere protein, ARK-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase complex, subunit Tim23 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase complex, subunit Tim23 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Inner nuclear membrane protein MAN1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Inner nuclear membrane protein MAN1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane protease subunit 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane protease subunit 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane protein Mitofilin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane protein Mitofilin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim16 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim16 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial import inner membrane translocase subunit Tim50 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial import inner membrane translocase subunit Tim50 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase complex, subunit Tim17 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase complex, subunit Tim17 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial inner membrane translocase subunit Tim17/Tim22/Tim23/peroxisomal protein PMP24 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

organelle inner membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the organelle inner membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

mitochondrial inner membrane Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the mitochondrial inner membrane cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

abnormal retinal inner nuclear layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations 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.

cochlear inner hair cell degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cochlear inner hair cell degeneration 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.

absent hair follicle inner root sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hair follicle inner root sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

inner cell mass degeneration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear inner hair cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner cell mass proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent retinal inner plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal orientation of inner hair cell stereociliary bundles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal orientation of inner hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner hair cell kinocilium morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased inner cell mass proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small inner medullary pyramid Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial inner membrane morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inner cell mass proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner hair cell stereocilia 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 inner cell mass apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner cell mass apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner hair cell synaptic ribbon morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner hair cell synaptic ribbon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent inner hair cell kinocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent inner hair cell kinocilia 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.

absent cochlear inner hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cochlear inner hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal inner nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cochlear inner hair cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

decreased cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fused inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fused inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased inner hair cell stereocilia number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized inner root sheath cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized inner root sheath cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney outer medulla inner stripe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney outer medulla inner stripe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin hair follicle inner rooth sheath Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin hair follicle inner rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin retinal inner plexiform layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal inner cell mass morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal inner cell mass 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 kidney inner medulla morphology Gene Set

From MPO Gene-Phenotype Associations

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

absent active-zone-anchored inner hair cell synaptic ribbon Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent active-zone-anchored inner hair cell synaptic ribbon 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.

absent inner cell mass Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retina inner limiting membrane morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retina inner limiting membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal inner plexiform layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal inner nuclear layer thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal inner nuclear layer thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized retinal inner nuclear layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle inner root sheath morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle inner root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased inner cell mass apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased inner cell mass apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

renal inner medulla Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue renal inner medulla in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner nuclear layer Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner nuclear layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner hair cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner medullary collecting duct Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner medullary collecting duct in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

hair follicle inner root sheath Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue hair follicle inner root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner dental epithelium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner dental epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner plexiform layer Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner plexiform layer in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner medullary collecting duct cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner medullary collecting duct cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

inner chondrogenic layer of perichondrium Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue inner chondrogenic layer of perichondrium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Focal dermal hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Focal dermal hypoplasia 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.

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.

Fibular hypoplasia and complex brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tibia, hypoplasia of, with polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tibia, hypoplasia of, with polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hypoplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype 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.

Pontocerebellar hypoplasia, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic nerve hypoplasia, bilateral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic nerve hypoplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Splenic hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Splenic hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Olivopontocerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Olivopontocerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia, type 1b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia, type 2e Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 2e phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Focal Dermal Hypoplasia Gene Set

From CTD Gene-Disease Associations

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

Fibular hypoplasia and complex brachydactyly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.

Cartilage-hair hypoplasia Gene Set

From CTD Gene-Disease Associations

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

Leydig Cell Hypoplasia Gene Set

From CTD Gene-Disease Associations

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

Optic Nerve Hypoplasia, Bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Nerve Hypoplasia, Bilateral from the curated CTD Gene-Disease Associations dataset.

Polymicrogyria With Optic Nerve Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polymicrogyria With Optic Nerve Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2C from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2B from the curated CTD Gene-Disease Associations dataset.

ADRENAL HYPOPLASIA, CONGENITAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset.

Anophthalmia with pulmonary hypoplasia Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 6 from the curated CTD Gene-Disease Associations dataset.

PONTOCEREBELLAR HYPOPLASIA, TYPE 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PONTOCEREBELLAR HYPOPLASIA, TYPE 4 from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 3 from the curated CTD Gene-Disease Associations dataset.

Iris hypoplasia and glaucoma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset.

Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2A from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance 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.

focal dermal hypoplasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

dental enamel hypoplasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

focal dermal hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cartilage-hair hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pituitary hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

dental enamel hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypoplasia Gene Set

From GeneRIF Biological Term Annotations

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

Primary pulmonary hypoplasia_Lung Tissue_GSE1363 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Primary pulmonary hypoplasia_Lung Tissue_GSE1363 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

aplasia/hypoplasia involving the central nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

aplasia/hypoplasia of the cerebrum Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the aplasia/hypoplasia of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

retinal hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of choroid Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the eye Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the fallopian tube Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of lymphatic vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the musculature Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the uvula Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tragus Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the nose Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the frontal sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

parathyroid hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the lungs Gene Set

From HPO Gene-Disease Associations

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

pancreatic hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the quadriceps Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the scapulae Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the ventral pons Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ventral pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

glenoid fossa hypoplasia Gene Set

From HPO Gene-Disease Associations

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

lymph node hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the skin Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of toe Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the iris Gene Set

From HPO Gene-Disease Associations

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

posterior vertebral hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the lacrimal puncta Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the lacrimal puncta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pyramidal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving forearm bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the sternum Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the optic nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ovary Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the phalanges of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the corticospinal tracts Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of penis Gene Set

From HPO Gene-Disease Associations

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

optic disc hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the tarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the thymus Gene Set

From HPO Gene-Disease Associations

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

thyroid hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the ulna Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving bones of the feet Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the primary teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the biceps Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia affecting the fundus Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia affecting the retina Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the hallux Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the odontoid process Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

calf muscle hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the gallbladder Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the pelvis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the mandible Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the epiglottis Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of metatarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of metatarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the uterus Gene Set

From HPO Gene-Disease Associations

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

erythroid hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the eyebrow Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the pons Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the spleen Gene Set

From HPO Gene-Disease Associations

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

breast hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the choroid Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the ciliary body Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the corpus callosum Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary hypoplasia Gene Set

From HPO Gene-Disease Associations

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

cerebellar hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving bones of the lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the brainstem Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the bladder Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the triceps Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the pharynx Gene Set

From HPO Gene-Disease Associations

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

macular hypoplasia Gene Set

From HPO Gene-Disease Associations

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

pectoralis hypoplasia Gene Set

From HPO Gene-Disease Associations

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

midclavicular hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal hypoplasia/aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the renal hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the femoral head Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mandibular condyle hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia affecting bones of the axial skeleton Gene Set

From HPO Gene-Disease Associations

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

corticospinal tract hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the 1st metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

carpal bone hypoplasia Gene Set

From HPO Gene-Disease Associations

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

distal ulnar hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the earlobes Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the calcaneus Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the 4th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of fingers Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the radius Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of proximal fibula Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of proximal fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of deltoid muscle Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of deltoid muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the thymus Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the 2nd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 2nd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the skeleton Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the ulna Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the uterus Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the humerus Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the palmar creases Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the maxilla Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the ribs Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the 1st metatarsal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 1st metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the vertebral column Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

laryngeal hypoplasia Gene Set

From HPO Gene-Disease Associations

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

lacrimal gland hypoplasia Gene Set

From HPO Gene-Disease Associations

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

frontal bone hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the metacarpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nipples Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the 5th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the capital femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the diaphragm Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the premaxilla Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the cerebrum Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the 3rd toe Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the bladder Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia affecting the uvea Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the sweat glands Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

unilateral breast hypoplasia Gene Set

From HPO Gene-Disease Associations

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

thoracic hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the femur Gene Set

From HPO Gene-Disease Associations

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

pectoralis major hypoplasia Gene Set

From HPO Gene-Disease Associations

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

adrenal medullary hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenal medullary hypoplasia 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.

hypoplasia of teeth Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the testes Gene Set

From HPO Gene-Disease Associations

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

labial hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving bones of the thorax Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the maxilla Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the optic tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nails Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the corpus callosum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inferior vermis hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the brainstem Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the fovea Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the cochlea Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the semicircular canal Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the femoral head and neck Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

external genital hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the vagina Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of first ribs Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of first ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar hemisphere hypoplasia Gene Set

From HPO Gene-Disease Associations

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

gonadal hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the iris Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the extremities Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the nasal septum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

2nd-5th toe middle phalangeal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the 2nd-5th toe middle phalangeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the clavicles Gene Set

From HPO Gene-Disease Associations

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

cerebellar vermis hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the sacrum Gene Set

From HPO Gene-Disease Associations

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

adrenocortical hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving bones of the skull Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the ovary Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the musculature of the pelvis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized cerebral atrophy/hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tibia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the prostate Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of proximal radius Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of proximal radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the patella Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the lesser trochanter Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the lesser trochanter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the skeletal musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the skeletal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the eyelid Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the vagina Gene Set

From HPO Gene-Disease Associations

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

unilateral chest hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the breasts Gene Set

From HPO Gene-Disease Associations

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

vertebral hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the musculature of the extremities Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

shoulder muscle hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the pyramidal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pancreas Gene Set

From HPO Gene-Disease Associations

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

cerebral hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the cochlea Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the fovea Gene Set

From HPO Gene-Disease Associations

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

optic nerve hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the cervical spine Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cerebellum Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the carpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenal hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hemifacial hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of dental enamel Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of dental enamel phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the lens Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the lens 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.

aplasia/hypoplasia involving the shoulder musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the frontal lobes Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the frontal lobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

scrotal hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the radius Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the capital femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the vertebrae Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving the musculature of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the fallopian tube Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tongue Gene Set

From HPO Gene-Disease Associations

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

upper limb muscle hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the upper limb muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patellar hypoplasia Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the epiglottis Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the colon Gene Set

From HPO Gene-Disease Associations

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

fibular hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the 3rd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pectoral muscle hypoplasia/aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the pectoral muscle hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary artery hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the macula Gene Set

From HPO Gene-Disease Associations

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

hypoplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paranasal sinus hypoplasia Gene Set

From HPO Gene-Disease Associations

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

clitoral hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the musculature of the thigh Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the musculature of the thigh phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the fibula Gene Set

From HPO Gene-Disease Associations

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

olivopontocerebellar hypoplasia Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the thumb Gene Set

From HPO Gene-Disease Associations

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

axillary apocrine gland hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the axillary apocrine gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Dental Enamel Hypoplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

testis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

tongue hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

genital tubercle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

lymphoid hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

palatine bone horizontal plate hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the palatine bone horizontal plate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thyroid hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

hindbrain hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

midface hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

intervertebral disk hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

lymph node hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

aortic arch hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pituitary intermediate lobe hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pituitary intermediate lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

temporal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

iris stroma hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ischium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

oviduct hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

spleen hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

radius hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

otic vesicle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

malleus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

maxilla hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

uterine cervix hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

adrenal gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

palatal shelf hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ventricle myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

leydig cell hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

mammary gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

scrotum hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

diencephalon hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

cochlear ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

frontal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

head mesenchyme hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

myometrium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

papillary muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

cerebellum vermis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

sebaceous gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

premaxilla hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

atrium myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pulmonary hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

female preputial gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pharyngeal arch artery hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

epididymis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

parathyroid hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

olfactory bulb hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

aorta hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

heart hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ethmoturbinate hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

hyoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pituitary gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

parietal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

axial mesoderm hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

mesangial cell hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

liver hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

palatine bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pancreas hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

gonial bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

conotruncal ridge hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

adenohypophysis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

renal hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

alisphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

vascular smooth muscle cell hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vascular smooth muscle cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hypaxial muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

basisphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pterygoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

endometrium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

vagina hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

dorsal root ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dorsal root ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aorta tubular hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

metacarpal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

axial skeleton hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

submandibular gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

myocardial trabeculae hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

vas deferens hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

cerebellum hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

sinus venosus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

kidney medulla hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pubis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ascending aorta hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

mandible hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

midbrain hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

nasal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

kidney cortex hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

maxillary shelf hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

rathke's pouch hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the rathke's pouch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

clavicle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

sertoli cell hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

eyelid hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

turbinate hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

vertebral body hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pulmonary trunk hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pancreatic acinar hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

vestibular ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

clitoris hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

placental labyrinth hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pharyngeal arch hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ovary hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

exocrine pancreas hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ureter hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

glossopharyngeal nerve hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

telencephalon hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

forebrain hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

scapular bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pancreatic islet hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

seminal vesicle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pharynx hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

trachea hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

thymus cortex hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

palate bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ventricular myocardium compact layer hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular myocardium compact layer hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vomer bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

optic nerve hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

meibomian gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

ventricular hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

interparietal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

uterus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

esophagus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

stomach hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

lateral prostate gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lateral prostate gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

atrium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

bulbourethral gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

philtrum hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

presphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

skeletal muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

heart right ventricle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart right ventricle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

urinary bladder hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

trabecula carnea hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

kidney papillary hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

gonadal ridge hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

pulmonary artery hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

sternum hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

otic capsule hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

retina hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

prostate gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

thymus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

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

iris hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the iris hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype 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.

pontocerebellar hypoplasia, type 2e Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

leydig cell hypoplasia with hypergonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leydig cell hypoplasia with hypergonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

leydig cell hypoplasia with pseudohermaphroditism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leydig cell hypoplasia with pseudohermaphroditism phenotype from the curated OMIM Gene-Disease Associations dataset.

hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

iris hypoplasia and glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the iris hypoplasia and glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.

mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities 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.

adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

focal dermal hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal dermal hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

foveal hypoplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic nerve hypoplasia and abnormalities of the central nervous system Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated OMIM Gene-Disease Associations dataset.

patella aplasia or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the patella aplasia or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 1c Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 1c phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

renal hypoplasia, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal hypoplasia, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

polymicrogyria with optic nerve hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the polymicrogyria with optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

?breasts and/or nipples, aplasia or hypoplasia of, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?breasts and/or nipples, aplasia or hypoplasia of, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic nerve hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

cartilage-hair hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cartilage-hair hypoplasia 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.

alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis phenotype from the curated OMIM Gene-Disease Associations dataset.