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Ontology Browser

Parent Terms Term With Siblings Child Terms
Deafness +     
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome  
Absence of Tibia with Congenital Deafness 
Albinism Deafness Syndrome 
Arthrogryposis Multiplex with Deafness, Inguinal Hernias, and Early Death 
autosomal dominant keratitis-ichthyosis-deafness syndrome  
autosomal dominant nonsyndromic deafness 65  
Ayazi Syndrome 
Branchiogenic-Deafness Syndrome 
Burn-Mckeown Syndrome  
Cardioauditory Syndrome of Sanchez Cascos 
Congenital Deafness and Familial Myoclonic Epilepsy 
Congenital Deafness, and Onychodystrophy, Autosomal Dominant  
Congenital Deafness, with Vitiligo and Achalasia 
Congenital Emphysema, with Deafness, Penoscrotal Web, and Mental Retardation 
Congenital Myopathy with Neuropathy and Deafness  
Coxoauricular Syndrome 
Davenport Donlan Syndrome 
Deaf-Blind Disorders +   
Deafness Hyperuricemia Neurologic Ataxia 
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
Deafness, Congenital Onychodystrophy, Recessive Form 
Deafness, Nonsyndromic, Modifier 1  
Deafness, with Smith-Magenis Syndrome  
Deafness, X-Linked 6  
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
Epiphyseal Dysplasia of Femoral Head, Myopia, and Deafness 
Fine-Lubinsky Syndrome 
Fountain Syndrome 
hereditary spastic paraplegia 24 
Herrmann Syndrome 
Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness 
Hyperlipoproteinemia Type II, and Deafness 
Ichthyosiform Erythroderma, Corneal Involvement, Deafness 
ITM2B-related cerebral amyloid angiopathy 2  
Johnson Neuroectodermal Syndrome 
Jones Syndrome 
Konigsmark Knox Hussels Syndrome 
Lynch Lee Murday syndrome 
Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome  
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1  
Meyenburg-Altherr-Uehlinger Syndrome 
Microcephaly Deafness Syndrome 
Muckle-Wells syndrome  
Multiple Synostoses Syndrome 1  
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonus, Cerebellar Ataxia, and Deafness 
Nasodigitoacoustic Syndrome  
Nathalie Syndrome 
Nephrosis Deafness Urinary Tract Digital Malformation 
Noninsulin-Dependent Diabetes Mellitus with Deafness  
nonsyndromic deafness +   
An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms. (DO)
Opticocochleodentate Degeneration 
Perrault syndrome +   
Ramos Arroyo Clark Syndrome 
Ribbonlike Corneal Degeneration with Deafness 
Richards-Rundle Syndrome 
Schimke X-Linked Mental Retardation Syndrome 
Schlegelberger Grote Syndrome 
Secretory Diarrhea, Myopathy, and Deafness 
Sinoatrial Node Dysfunction and Deafness  
temtamy preaxial brachydactyly syndrome  
Tietz syndrome  
Wells Jankovic Syndrome 
Wright Dyck Syndrome 
X-linked Alport syndrome  
X-Linked Mental Retardation Gustavson Type 
X-Linked Retinitis Pigmentosa, and Sinorespiratory Infections, with or without Deafness  
Y-Linked Deafness +   
Yemenite Deaf-Blind Hypopigmentation Syndrome 

Exact Synonyms: Isolated Deafness ;   Nonsyndromic Hearing Impairment ;   Nonsyndromic Hearing Loss ;   Undifferentiated Deafness ;   nonsyndromic hereditary hearing loss
Narrow Synonyms: Non-syndromic Genetic Deafness ;   Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive
Primary IDs: MESH:C580334 ;   RDO:0015912
Definition Sources:,,

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.