| Disease Browser
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Parent Node:
 Hearing Loss (D034381) | ..Starting node
.. Hearing Loss, Bilateral (D006312)
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Child Nodes:
| | ........Bagatelle Cassidy syndrome (C537796) | | ........Feigenbaum Bergeron Richardson syndrome (C536178) | | ........Forney Robinson Pascoe syndrome (C537269) | | ........Hagemoser Weinstein Bresnick syndrome (C537626) | | ........Oculootoradial syndrome (C535544) |
Sister Nodes: | ..Abidi X-linked mental retardation syndrome (C535556)
| ..Behr syndrome (C537669)
| ..Branchial arch syndrome X-linked (C537102)
| ..CATSHL syndrome (C537975)
| ..Chromosome 6pter-P24 Deletion Syndrome (C567239)
| ..Deafness (D003638)  108
| ..Deafness with Anhidrotic Ectodermal Dysplasia (C565119)
| ..Deafness, Autosomal Dominant, Due To Mutation In Myo1a (C567266)
| ..Deafness, Autosomal Recessive 36, Without Vestibular Involvement (C567219)
| ..Deafness, Congenital Heart Defects, and Posterior Embryotoxon (C566604)
| ..Deafness, Unilateral, With Delayed Endolymphatic Hydrops (C567420)
| ..Deafness-Craniofacial Syndrome (C565118)
| ..Hearing Loss, Bilateral (D006312) 5
| ..HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO (OMIM:613290)
| ..Hearing Loss, Conductive (D006314) 21
| ..Hearing Loss, Functional (D006315)
| ..Hearing Loss, High-Frequency (D006316)
| ..Hearing Loss, Mixed Conductive-Sensorineural (D046089) 3
| ..Hearing Loss, Sensorineural (D006319) 252
| ..Hearing Loss, Sudden (D003639)
| ..Hearing Loss, Unilateral (D046088) 1
| ..Iris dysplasia hypertelorism deafness (C535537)
| ..Lacrimoauriculodentodigital syndrome (C538132)
| ..Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance (C567849)
| ..Microtia, Hearing Impairment, And Cleft Palate (C567359)
| ..Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay (C567769)
| ..Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497)
| ..Reardon Wilson Cavanagh syndrome (C535295)
| ..Spondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness (C566507)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 4922 |
| Name: | Hearing Loss, Bilateral |
| Definition: | Partial hearing loss in both ears. |
| Alternative IDs: | |
| ParentIDs: | MESH:D034381 |
| TreeNumbers: | C09.218.458.341.374 |C10.597.751.418.341.374 |C23.888.592.763.393.341.374 |
| Synonyms: | Bilateral Hearing Loss |Bilateral Hearing Losses |Hearing Losses, Bilateral |Loss, Bilateral Hearing |Losses, Bilateral Hearing |
| Slim Mappings: | Ear-nose-throat disease|Nervous system disease|Signs and symptoms |
| Reference: |
MedGen: D006312
MeSH: D006312
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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