Name

Gonadal Dysgenesis Gene Set

From CTD Gene-Disease Associations

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

gonadal dysgenesis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

gonadal dysgenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gonadal dysgenesis Gene Set

From GWASdb SNP-Disease Associations

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

gonadal dysgenesis Gene Set

From HPO Gene-Disease Associations

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

Gonadal Dysgenesis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

46,XY gonadal dysgenesis, partial, with minifascicular neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

46,XY gonadal dysgenesis, complete, dhh-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY gonadal dysgenesis, complete, dhh-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gonadal Dysgenesis, 46,XX Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gonadal Dysgenesis, 46,XX from the curated CTD Gene-Disease Associations dataset.

46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related from the curated CTD Gene-Disease Associations dataset.

46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy from the curated CTD Gene-Disease Associations dataset.

Gonadal Dysgenesis, 46,XY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gonadal Dysgenesis, 46,XY from the curated CTD Gene-Disease Associations dataset.

Gonadal dysgenesis XX type deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gonadal dysgenesis XX type deafness from the curated CTD Gene-Disease Associations dataset.

46 xy gonadal dysgenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease 46 xy gonadal dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mixed gonadal dysgenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gonadal dysgenesis, 46,xy; infertility, male; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gonadal dysgenesis, 46,xy; infertility, male; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gonadal dysgenesis, 46,xy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gonadal dysgenesis, 46,xy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gonadal dysgenesis, male Gene Set

From HPO Gene-Disease Associations

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

Gonadal Dysgenesis, 46,XY Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Gonadal Dysgenesis, 46,XY phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

46xy partial gonadal dysgenesis, with minifascicular neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the 46xy partial gonadal dysgenesis, with minifascicular neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

Gonadal Steroid Hormones Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Gonadal Steroid Hormones from the curated CTD Gene-Chemical Interactions dataset.

Gonadal Disorders Gene Set

From CTD Gene-Disease Associations

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

gonadal disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

gonadal disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

sex cord-gonadal stromal tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sex cord-gonadal stromal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

gonadal steroids and lipid levels Gene Set

From GAD Gene-Disease Associations

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

gonadal Gene Set

From GeneRIF Biological Term Annotations

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

gonadal mesoderm development Gene Set

From GO Biological Process Annotations

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

gonadal disease Gene Set

From GWASdb SNP-Disease Associations

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

puberty and gonadal disorders Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the puberty and gonadal disorders phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

gonadal neoplasm Gene Set

From GWASdb SNP-Phenotype Associations

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

puberty and gonadal disorders Gene Set

From HPO Gene-Disease Associations

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

gonadal tissue inappropriate for external genitalia or chromosomal sex Gene Set

From HPO Gene-Disease Associations

genes associated with the gonadal tissue inappropriate for external genitalia or chromosomal sex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

primary gonadal insufficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the primary gonadal insufficiency 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.

gonadal neoplasm Gene Set

From HPO Gene-Disease Associations

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

Neoplasms, Gonadal Tissue Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neoplasms, Gonadal Tissue phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Sex Cord-Gonadal Stromal Tumors Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Sex Cord-Gonadal Stromal Tumors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

decreased gonadal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased gonadal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal gonadal ridge morphology Gene Set

From MPO Gene-Phenotype Associations

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

increased gonadal fat pad weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased gonadal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal gonadal fat pad morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal gonadal fat pad morphology 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.

Irido-corneo-trabecular dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Irido-corneo-trabecular dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

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.

Reticular dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Reticular dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ovarian dysgenesis 1 Gene Set

From ClinVar Gene-Phenotype Associations

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

Ovarian dysgenesis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ovarian dysgenesis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anterior segment mesenchymal dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

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

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.

OVARIAN DYSGENESIS 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OVARIAN DYSGENESIS 1 from the curated CTD Gene-Disease Associations dataset.

Athabaskan brainstem dysgenesis Gene Set

From CTD Gene-Disease Associations

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

Anterior segment mesenchymal dysgenesis Gene Set

From CTD Gene-Disease Associations

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

RENAL TUBULAR DYSGENESIS Gene Set

From CTD Gene-Disease Associations

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

Reticular dysgenesis Gene Set

From CTD Gene-Disease Associations

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

Ovarian Dysgenesis 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ovarian Dysgenesis 2 from the curated CTD Gene-Disease Associations dataset.

Sudden Infant Death with Dysgenesis of the Testes Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sudden Infant Death with Dysgenesis of the Testes Syndrome 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.

reticular dysgenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypothyroidism; thyroid dysgenesis Gene Set

From GAD Gene-Disease Associations

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

thyroid dysgenesis Gene Set

From GAD Gene-Disease Associations

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

congenital abnormalities; hypothyroidism; thyroid dysgenesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital abnormalities; hypothyroidism; thyroid dysgenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital hypothyroidism; thyroid dysgenesis Gene Set

From GAD Gene-Disease Associations

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

dysgenesis Gene Set

From GeneRIF Biological Term Annotations

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

testicular dysgenesis Gene Set

From GWASdb SNP-Phenotype Associations

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

thyroid dysgenesis Gene Set

From HPO Gene-Disease Associations

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

testicular dysgenesis Gene Set

From HPO Gene-Disease Associations

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

adrenal gland dysgenesis Gene Set

From HPO Gene-Disease Associations

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

unilateral primary pulmonary dysgenesis Gene Set

From HPO Gene-Disease Associations

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

posterior pituitary dysgenesis Gene Set

From HPO Gene-Disease Associations

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

renotubular dysgenesis Gene Set

From HPO Gene-Disease Associations

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

dysgenesis of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

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

intrahepatic biliary dysgenesis Gene Set

From HPO Gene-Disease Associations

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

anterior segment dysgenesis Gene Set

From HPO Gene-Disease Associations

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

anterior pituitary dysgenesis Gene Set

From HPO Gene-Disease Associations

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

parathyroid dysgenesis Gene Set

From HPO Gene-Disease Associations

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

Thyroid Dysgenesis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From OMIM Gene-Disease Associations

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

anterior segment mesenchymal dysgenesis Gene Set

From OMIM Gene-Disease Associations

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

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.

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.

ovarian dysgenesis 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ovarian dysgenesis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ovarian dysgenesis 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ovarian dysgenesis 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ovarian dysgenesis 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ovarian dysgenesis 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

sudden infant death with dysgenesis of the testes syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the sudden infant death with dysgenesis of the testes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

athabaskan brainstem dysgenesis syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the athabaskan brainstem dysgenesis syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

renal tubular dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

reticular dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the reticular dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.