Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandHearing Loss (D034381)
..Starting node
..expandHearing Loss, Mixed Conductive-Sensorineural (D046089)

       Child Nodes:
........expandDeafness-Hypogonadism Syndrome (C564435)
........expandFacial Dysmorphism, Cleft Palate, Hearing Loss, and Camptodactyly (C566524)
........expandHypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss (C566373)



 Sister Nodes: 
..expandAbidi X-linked mental retardation syndrome (C535556)
..expandBehr syndrome (C537669)
..expandBranchial arch syndrome X-linked (C537102)
..expandCATSHL syndrome (C537975)
..expandChromosome 6pter-P24 Deletion Syndrome (C567239)
..expandDeafness (D003638) Child108
..expandDeafness with Anhidrotic Ectodermal Dysplasia (C565119)
..expandDeafness, Autosomal Dominant, Due To Mutation In Myo1a (C567266)
..expandDeafness, Autosomal Recessive 36, Without Vestibular Involvement (C567219)
..expandDeafness, Congenital Heart Defects, and Posterior Embryotoxon (C566604)
..expandDeafness, Unilateral, With Delayed Endolymphatic Hydrops (C567420)
..expandDeafness-Craniofacial Syndrome (C565118)
..expandHearing Loss, Bilateral (D006312) Child5
..expandHEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO (OMIM:613290)
..expandHearing Loss, Conductive (D006314) Child21
..expandHearing Loss, Functional (D006315)
..expandHearing Loss, High-Frequency (D006316)
..expandHearing Loss, Mixed Conductive-Sensorineural (D046089) Child3
..expandHearing Loss, Sensorineural (D006319) Child252
..expandHearing Loss, Sudden (D003639)
..expandHearing Loss, Unilateral (D046088) Child1
..expandIris dysplasia hypertelorism deafness (C535537)
..expandLacrimoauriculodentodigital syndrome (C538132)
..expandMicrocephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance (C567849)
..expandMicrotia, Hearing Impairment, And Cleft Palate (C567359)
..expandMyopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay (C567769)
..expandOptic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497)
..expandReardon Wilson Cavanagh syndrome (C535295)
..expandSpondylomegaepiphyseal Dysplasia With Upper Limb Mesomelia, Punctate Calcifications, And Deafness (C566507)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:4928
Name:Hearing Loss, Mixed Conductive-Sensorineural
Definition:Hearing loss due to damage or impairment of both the conductive elements (HEARING LOSS, CONDUCTIVE) and the sensorineural elements (HEARING LOSS, SENSORINEURAL) of the ear.
Alternative IDs:
ParentIDs:MESH:D034381
TreeNumbers:C09.218.458.341.849 |C10.597.751.418.341.849 |C23.888.592.763.393.341.849
Synonyms:Hearing Loss, Mixed |Hearing Loss, Mixed Conductive Sensorineural |Losses, Mixed Hearing |Loss, Mixed Hearing |Mixed Hearing Loss
Slim Mappings:Ear-nose-throat disease|Nervous system disease|Signs and symptoms
Reference: MedGen: D046089
MeSH: D046089
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants