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Metadata
ID	DOID:0110593
Name	autosomal dominant nonsyndromic deafness 9
Definition	An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/9806553
Xrefs	ICD10CM:H90.3 MIM:601369
Synonyms	autosomal dominant deafness 9 [EXACT] DFNA9 [EXACT]
Parent Relationships	is_a autosomal dominant nonsyndromic deafness