| Disease Browser
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Parent Node:
 Hearing Disorders (D006311) | ..Starting node
.. Hearing Loss (D034381)
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Child 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) |
Sister Nodes: | ..Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia (C580009)
| ..Hearing Loss (D034381) 397
| ..Hyperacusis (D012001)
| ..Ossicular Malformations, familial (C537142)
| ..Tinnitus (D014012) 1
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 4921 |
| Name: | Hearing Loss |
| Definition: | A general term for the complete or partial loss of the ability to hear from one or both ears. |
| Alternative IDs: | |
| ParentIDs: | MESH:D006311 |
| TreeNumbers: | C09.218.458.341 |C10.597.751.418.341 |C23.888.592.763.393.341 |
| Synonyms: | Hearing Impairment |Hypoacuses |Hypoacusis |Loss, Hearing |
| Slim Mappings: | Ear-nose-throat disease|Nervous system disease|Signs and symptoms |
| Reference: |
MedGen: D034381
MeSH: D034381
OMIM:
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
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