Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Hearing Loss +     
ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS  
Behr Syndrome  
Branchial Arch Syndrome X-Linked 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
chromosome 6pter-p24 deletion syndrome 
Conductive Hearing Loss +   
Cone-Rod Dystrophy and Hearing Loss +   
Congenital Cataracts, Hearing Loss, and Neurodegeneration  
Deafness +   
A general term for the complete loss of the ability to hear from both ears.
Deafness with Anhidrotic Ectodermal Dysplasia 
Deafness, Autosomal Dominant, due to Mutation In Myo1a 
Deafness, Congenital Heart Defects, and Posterior Embryotoxon  
Deafness, Unilateral, with Delayed Endolymphatic Hydrops  
Deafness-Craniofacial Syndrome 
EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2  
Epilepsy, Hearing Loss, and Mental Retardation Syndrome  
Functional Hearing Loss 
Hearing Loss, Bilateral +   
Hearing Loss, Mixed Conductive-Sensorineural +  
Hearing Loss, Unilateral +   
High-Frequency Hearing Loss  
Iris Dysplasia Hypertelorism Deafness 
LADD syndrome  
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance 
Microtia, Hearing Impairment, and Cleft Palate  
MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS  
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant 
Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss  
Reardon Wilson Cavanagh Syndrome 
sensorineural hearing loss +   
SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES  
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
syndromic X-linked intellectual disability Abidi type 
Uveal Coloboma, with Cleft Lip and Palate and Mental Retardation  

Synonyms
Exact Synonyms: Acquired Deafness ;   Bilateral Deafness ;   Complete Hearing Loss ;   Deaf Mutism ;   Extreme Hearing Loss ;   Prelingual Deafness
Primary IDs: MESH:D003638 ;   RDO:0000298
Definition Sources: MESH:D003638

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