Name

bilateral conductive hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the bilateral conductive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, high-frequency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, high-frequency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete hearing loss; deafness; hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

conductive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

progressive conductive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

conductive hearing impairment Gene Set

From MPO Gene-Phenotype Associations

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

bilateral sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the bilateral sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

complete hearing loss; deafness; hearing loss, bilateral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; hearing loss, bilateral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, bilateral; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, bilateral; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; otosclerosis Gene Set

From GAD Gene-Disease Associations

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

hearing impairment; hearing loss; infant, premature, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; infant, premature, diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic diseases, inborn; hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic diseases, inborn; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

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

eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing disorders; hearing loss, high-frequency; hearing problem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing disorders; hearing loss, high-frequency; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete hearing loss; deafness; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Hearing Loss, Conductive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Conductive from the curated CTD Gene-Disease Associations dataset.

Hearing Loss, Mixed Conductive-Sensorineural Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Mixed Conductive-Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

conductive hearing loss Gene Set

From MPO Gene-Phenotype Associations

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

Hearing Loss, Bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Bilateral from the curated CTD Gene-Disease Associations dataset.

hearing loss, bilateral Gene Set

From GAD Gene-Disease Associations

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

Hearing Loss, Bilateral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Bilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hearing impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, Hearing Impairment, And Cleft Palate Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.

Age-Related Hearing Impairment 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Age-Related Hearing Impairment 1 from the curated CTD Gene-Disease Associations dataset.

hearing impairment Gene Set

From GAD Gene-Disease Associations

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

nonsyndromic hearing impairment Gene Set

From GAD Gene-Disease Associations

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

Age-related hearing impairment (interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related hearing impairment (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related hearing impairment Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Hearing impairment Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

hearing impairment Gene Set

From GWASdb SNP-Phenotype Associations

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

high-frequency hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the high-frequency hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

hearing impairment Gene Set

From HPO Gene-Disease Associations

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

sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

low-frequency sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the low-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

prelingual sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the prelingual sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

postlingual sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the postlingual sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mild hearing impairment Gene Set

From HPO Gene-Disease Associations

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

mild neurosensory hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the mild neurosensory hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

infantile sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the infantile sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

profound hearing impairment Gene Set

From HPO Gene-Disease Associations

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

progressive sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

childhood onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe hearing impairment Gene Set

From HPO Gene-Disease Associations

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

high-frequency sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the high-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mixed hearing impairment Gene Set

From HPO Gene-Disease Associations

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

severe sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the severe sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adult onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the adult onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

profound sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the profound sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sensorineural hearing impairment Gene Set

From MPO Gene-Phenotype Associations

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

nonsyndromic hearing impairment Gene Set

From MPO Gene-Phenotype Associations

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

syndromic hearing impairment Gene Set

From MPO Gene-Phenotype Associations

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

?microtia, hearing impairment, and cleft palate (ar) Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microtia, hearing impairment, and cleft palate (ar) phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

{age-related hearing impairment 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {age-related hearing impairment 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{age-related hearing impairment 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {age-related hearing impairment 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

hearing loss; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; sensorineural hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; sensorineural hearing loss; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hemoglobin sc disease; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hemoglobin sc disease; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem Gene Set

From GAD Gene-Disease Associations

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

hearing disorders; hearing problem; syndrome Gene Set

From GAD Gene-Disease Associations

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

deafness; hearing loss; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; hearing loss; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing disorders; hearing problem Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

conductive Gene Set

From GeneRIF Biological Term Annotations

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

Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polymicrogyria, bilateral frontoparietal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polymicrogyria, bilateral frontoparietal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cryptorchidism, unilateral or bilateral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cryptorchidism, unilateral or bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polymicrogyria, bilateral perisylvian, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polymicrogyria, bilateral perisylvian, autosomal recessive 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.

Optic nerve aplasia, bilateral Gene Set

From ClinVar Gene-Phenotype Associations

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

Polymicrogyria, bilateral occipital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polymicrogyria, bilateral occipital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital bilateral aplasia of vas deferens Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset.

Multicystic renal dysplasia, bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multicystic renal dysplasia, bilateral 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, Bilateral Occipital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polymicrogyria, Bilateral Occipital from the curated CTD Gene-Disease Associations dataset.

bilateral breast cancer Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

bilateral retinoblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

synchronous bilateral breast carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

congenital bilateral absence of the vas deferens Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital bilateral absence of the vas deferens in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bilateral iliac vein thrombosis Gene Set

From GAD Gene-Disease Associations

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

bilateral Gene Set

From GeneRIF Biological Term Annotations

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

determination of bilateral symmetry Gene Set

From GO Biological Process Annotations

genes participating in the determination of bilateral symmetry biological process from the curated GO Biological Process Annotations dataset.

Sensory disturbances after bilateral sagittal split ramus osteotomy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Sensory disturbances after bilateral sagittal split ramus osteotomy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

bilateral talipes equinovarus Gene Set

From HPO Gene-Disease Associations

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

bilateral intracranial calcifications Gene Set

From HPO Gene-Disease Associations

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

bilateral elbow dislocations Gene Set

From HPO Gene-Disease Associations

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

bilateral triphalangeal thumbs Gene Set

From HPO Gene-Disease Associations

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

congenital bilateral hip dislocation Gene Set

From HPO Gene-Disease Associations

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

bilateral cleft lip and palate Gene Set

From HPO Gene-Disease Associations

genes associated with the bilateral cleft lip and palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bilateral cleft palate Gene Set

From HPO Gene-Disease Associations

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

bilateral radial aplasia Gene Set

From HPO Gene-Disease Associations

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

bilateral single transverse palmar creases Gene Set

From HPO Gene-Disease Associations

genes associated with the bilateral single transverse palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bilateral camptodactyly Gene Set

From HPO Gene-Disease Associations

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

bilateral ptosis Gene Set

From HPO Gene-Disease Associations

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

bilateral coxa valga Gene Set

From HPO Gene-Disease Associations

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

bilateral cryptorchidism Gene Set

From HPO Gene-Disease Associations

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

bilateral microphthalmos Gene Set

From HPO Gene-Disease Associations

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

bilateral vestibular schwannoma Gene Set

From HPO Gene-Disease Associations

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

bilateral lung agenesis Gene Set

From HPO Gene-Disease Associations

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

bilateral basal ganglia lesions Gene Set

From HPO Gene-Disease Associations

genes associated with the bilateral basal ganglia lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bilateral cleft lip Gene Set

From HPO Gene-Disease Associations

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

bilateral convulsive seizures Gene Set

From HPO Gene-Disease Associations

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

?polymicrogyria, bilateral temporooccipital Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?polymicrogyria, bilateral temporooccipital phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital bilateral absence of vas deferens Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital bilateral absence of vas deferens phenotype from the curated OMIM Gene-Disease Associations dataset.

polymicrogyria, bilateral perisylvian Gene Set

From OMIM Gene-Disease Associations

genes associated with the polymicrogyria, bilateral perisylvian phenotype from the curated OMIM Gene-Disease Associations dataset.

polymicrogyria, bilateral occipital Gene Set

From OMIM Gene-Disease Associations

genes associated with the polymicrogyria, bilateral occipital phenotype from the curated OMIM Gene-Disease Associations dataset.

polymicrogyria, bilateral frontoparietal Gene Set

From OMIM Gene-Disease Associations

genes associated with the polymicrogyria, bilateral frontoparietal phenotype from the curated OMIM Gene-Disease Associations dataset.

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cognitive impairment with or without cerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

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

Deafness, cochlear, with myopia and intellectual impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SPECIFIC LANGUAGE IMPAIRMENT 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPECIFIC LANGUAGE IMPAIRMENT 2 from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

SPECIFIC LANGUAGE IMPAIRMENT 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPECIFIC LANGUAGE IMPAIRMENT 3 from the curated CTD Gene-Disease Associations dataset.

Specific Language Impairment 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Specific Language Impairment 4 from the curated CTD Gene-Disease Associations dataset.

SPECIFIC LANGUAGE IMPAIRMENT 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPECIFIC LANGUAGE IMPAIRMENT 1 from the curated CTD Gene-Disease Associations dataset.

Mild Cognitive Impairment Gene Set

From CTD Gene-Disease Associations

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

mild cognitive impairment Gene Set

From GAD Gene-Disease Associations

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

anxiety disorder; blood pressure, arterial; memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety disorder; blood pressure, arterial; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multidimensional impairment Gene Set

From GAD Gene-Disease Associations

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

memory impairment, subjective Gene Set

From GAD Gene-Disease Associations

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

memory impairment Gene Set

From GAD Gene-Disease Associations

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

cognitive impairment, vascular stroke, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cognitive impairment, vascular stroke, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anticholinergic challenge-induced memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anticholinergic challenge-induced memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

human spermatogenesis impairment Gene Set

From GAD Gene-Disease Associations

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

asthma; lipids; memory impairment Gene Set

From GAD Gene-Disease Associations

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

cognitive impairment; alzheimers disease Gene Set

From GAD Gene-Disease Associations

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

age-associated memory impairment Gene Set

From GAD Gene-Disease Associations

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

cognitive impairment Gene Set

From GAD Gene-Disease Associations

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

spermatogenic impairment Gene Set

From GAD Gene-Disease Associations

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

age-associated memory impairment (aami) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age-associated memory impairment (aami) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impairmentazoospermia Gene Set

From GeneRIF Biological Term Annotations

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

impairments Gene Set

From GeneRIF Biological Term Annotations

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

impairment Gene Set

From GeneRIF Biological Term Annotations

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

Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Parent of origin effect on language impairment (paternal) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Parent of origin effect on language impairment (paternal) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

neurological speech impairment Gene Set

From GWASdb SNP-Phenotype Associations

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

memory impairment Gene Set

From GWASdb SNP-Phenotype Associations

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

cognitive impairment Gene Set

From GWASdb SNP-Phenotype Associations

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

language impairment Gene Set

From GWASdb SNP-Phenotype Associations

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

focal seizures with impairment of consciousness or awareness Gene Set

From HPO Gene-Disease Associations

genes associated with the focal seizures with impairment of consciousness or awareness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

focal seizures without impairment of consciousness or awareness Gene Set

From HPO Gene-Disease Associations

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

cognitive impairment Gene Set

From HPO Gene-Disease Associations

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

language impairment Gene Set

From HPO Gene-Disease Associations

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

severe visual impairment Gene Set

From HPO Gene-Disease Associations

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

sensory impairment Gene Set

From HPO Gene-Disease Associations

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

memory impairment Gene Set

From HPO Gene-Disease Associations

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

progressive pulmonary function impairment Gene Set

From HPO Gene-Disease Associations

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

distal sensory impairment of all modalities Gene Set

From HPO Gene-Disease Associations

genes associated with the distal sensory impairment of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cortical visual impairment Gene Set

From HPO Gene-Disease Associations

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

neurological speech impairment Gene Set

From HPO Gene-Disease Associations

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

impairment of galactose metabolism Gene Set

From HPO Gene-Disease Associations

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

distal sensory impairment Gene Set

From HPO Gene-Disease Associations

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

impairment of fructose metabolism Gene Set

From HPO Gene-Disease Associations

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

visual impairment Gene Set

From HPO Gene-Disease Associations

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

mental retardation with language impairment and autistic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation with language impairment and autistic features phenotype from the curated OMIM Gene-Disease Associations dataset.

specific language impairment qtl, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the specific language impairment qtl, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

specific language impairment qtl, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the specific language impairment qtl, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cognitive impairment with or without cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

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

{specific language impairment 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {specific language impairment 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{memory impairment, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {memory impairment, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

specific language impairment qtl, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the specific language impairment qtl, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{specific language impairment 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {specific language impairment 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

DFNA 2 Nonsyndromic Hearing Loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the DFNA 2 Nonsyndromic Hearing Loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, and hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hearing Loss, Sudden Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Sudden from the curated CTD Gene-Disease Associations dataset.

Hearing Loss Gene Set

From CTD Gene-Disease Associations

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

HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Hearing Disorders Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Progressive hearing loss stapes fixation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive hearing loss stapes fixation from the curated CTD Gene-Disease Associations dataset.

Hearing Loss, Sensorineural Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Sensorineural from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Hearing Loss, Noise-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Noise-Induced from the curated CTD Gene-Disease Associations dataset.

Hearing Loss Gene Set

From dbGAP Gene-Trait Associations

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

sensorineural hearing loss Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss/deafness; osteogenesis imperfecta Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

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

complete hearing loss; deafness; vestibular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; vestibular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, central Gene Set

From GAD Gene-Disease Associations

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

autosomal dominant hearing loss Gene Set

From GAD Gene-Disease Associations

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

bone neoplasms; hearing loss; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; hearing loss; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural nonsyndromic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural nonsyndromic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

goiter; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease goiter; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dominant non-syndromic sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dominant non-syndromic sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss/deafness; retinal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; retinal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

goiter; hearing loss, sensorineural; vertigo Gene Set

From GAD Gene-Disease Associations

genes associated with the disease goiter; hearing loss, sensorineural; vertigo in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; hearing loss, sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, unilateral Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

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

hearing loss/deafness Gene Set

From GAD Gene-Disease Associations

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

nonsyndromic hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing disorders Gene Set

From GAD Gene-Disease Associations

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

hearing loss, nonsyndromic sensorineural Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, nonsyndromic sensorineural in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; hearing loss Gene Set

From GAD Gene-Disease Associations

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

goiter; hearing loss, sensorineural; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease goiter; hearing loss, sensorineural; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, noise-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, noise-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, noise-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sudden; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss; noonan syndrome Gene Set

From GAD Gene-Disease Associations

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

presbycusis; hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing Gene Set

From GeneRIF Biological Term Annotations

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

hearing abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

low-frequency hearing loss Gene Set

From HPO Gene-Disease Associations

genes associated with the low-frequency hearing loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hearing abnormality Gene Set

From HPO Gene-Disease Associations

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

Hearing Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Central Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Central phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Unilateral Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Unilateral phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, Functional Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Functional phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, Sensorineural Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Sensorineural phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, Noise-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Noise-Induced phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, High-Frequency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, High-Frequency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hearing Loss, Sudden Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, Sudden phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

syndromic hearing loss Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hearing physiology Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to ototoxicity-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ototoxicity-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sensorineural hearing loss Gene Set

From MPO Gene-Phenotype Associations

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

nonsyndromic hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the nonsyndromic hearing loss 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.

increased susceptibility to age-related hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to age-related hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired hearing Gene Set

From MPO Gene-Phenotype Associations

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

increased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hearing electrophysiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal susceptibility to hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

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

From OMIM Gene-Disease Associations

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

?split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

{?hearing loss, cisplatin-induced, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {?hearing loss, cisplatin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

congenital cataracts, hearing loss, and neurodegeneration Gene Set

From OMIM Gene-Disease Associations

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

?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.