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Metadata
ID	DOID:0110550
Name	autosomal dominant nonsyndromic deafness 20
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 ACTG1 gene on chromosome 17q25. https://www.ncbi.nlm.nih.gov/pubmed/13680526
Xrefs	ICD10CM:H90.3 OMIM:604717
Synonyms	autosomal dominant deafness 20 [EXACT] DFNA20 [EXACT] DFNA26 [EXACT]
Parent Relationships	is_a autosomal dominant nonsyndromic deafness