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Metadata
ID	DOID:0110576
Name	autosomal dominant nonsyndromic deafness 50
Definition	An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has_material_basis_in mutation in the MIRN96 gene on chromosome 7q32. https://www.ncbi.nlm.nih.gov/pubmed/19363479
Xrefs	ICD10CM:H90.3 MIM:613074
Synonyms	autosomal dominant deafness 50 [EXACT] DFNA50 [EXACT]
Parent Relationships	is_a autosomal dominant nonsyndromic deafness