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Metadata
ID	DOID:0110480
Name	autosomal recessive nonsyndromic deafness 22
Definition	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOA gene on chromosome 16p12. https://www.ncbi.nlm.nih.gov/pubmed/11972037
Xrefs	ICD10CM:H90.3 OMIM:607039
Synonyms	autosomal recessive deafness 22 [EXACT] DFNB22 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness