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Metadata
ID	DOID:0110552
Name	autosomal dominant nonsyndromic deafness 22
Definition	An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14. https://www.ncbi.nlm.nih.gov/pubmed/11468689
Xrefs	ICD10CM:H90.3 OMIM:606346
Synonyms	autosomal dominant deafness 22 [EXACT] DFNA22 [EXACT]
Parent Relationships	is_a autosomal dominant nonsyndromic deafness