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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 MIM:606705
Synonyms	autosomal dominant deafness 36 [EXACT] DFNA36 [EXACT]
Parent Relationships	is_a autosomal dominant nonsyndromic deafness