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Metadata
ID DOID:0110563
Name autosomal dominant nonsyndromic deafness 36
Definition An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21.
https://www.ncbi.nlm.nih.gov/pubmed/11850618
Xrefs

ICD10CM:H90.3

OMIM:606705

Synonyms

autosomal dominant deafness 36 [EXACT]

DFNA36 [EXACT]

Parent Relationships

is_a autosomal dominant nonsyndromic deafness

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