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, Conductive (D006314)

       Child Nodes:
........expandAbruzzo Erickson syndrome (C535559)
........expandCleft Palate, Deafness, and Oligodontia (C565844)
........expandDeafness conductive ptosis skeletal anomalies (C535993)
........expandDeafness, Cochlear, with Myopia and Intellectual Impairment (C565645)
........expandDeafness, Conductive Stapedial, with Ear Malformation and Facial Palsy (C565123)
........expandDeafness, Conductive, with Malformed External Ear (C565644)
........expandDeafness, Neural, with Atypical Atopic Dermatitis (C565639)
........expandDeafness, Progressive, With Stapes Fixation (C563316)
........expandEpiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness (C565046)
........expandGOMBO syndrome (C537284)
........expandMastocytosis, cutaneous, with short stature, conductive hearing loss and microtia (C536033)
........expandMengel Konigsmark syndrome (C537239)
........expandMetaphyseal Dysostosis, Mental Retardation, and Conductive Deafness (C565396)
........expandMicrotia, meatal atresia and conductive deafness (C537469)
........expandMitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones (C563572)
........expandProgressive hearing loss stapes fixation (C536424)
........expandRetinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism (C564841)
........expandSchweitzer Kemink Graham syndrome (C536511)
........expandSiegler Brewer Carey syndrome (C537335)
........expandStoll Levy Francfort syndrome (C537498)
........expandZunich neuroectodermal syndrome (C536729)



 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:4925
Name:Hearing Loss, Conductive
Definition:Hearing loss due to interference with the mechanical reception or amplification of sound to the COCHLEA. The interference is in the outer or middle ear involving the EAR CANAL; TYMPANIC MEMBRANE; or EAR OSSICLES.
Alternative IDs:
ParentIDs:MESH:D034381
TreeNumbers:C09.218.458.341.562 |C10.597.751.418.341.562 |C23.888.592.763.393.341.562
Synonyms:Conductive Hearing Loss
Slim Mappings:Ear-nose-throat disease|Nervous system disease|Signs and symptoms
Reference: MedGen: D006314
MeSH: D006314
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants