Disease Browser
|
Parent Node: Hearing Disorders (D006311) | ..Starting node This term CN229757 is not assigned on to the disease tree yet, Hearing Loss (4921) is shown instead. ..Hearing Loss (D034381)
| 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
|
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
|
|
|
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 | |
|