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Metadata
ID	DOID:0110495
Name	autosomal recessive nonsyndromic deafness 37
Definition	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14. https://www.ncbi.nlm.nih.gov/pubmed/12687499
Xrefs	ICD10CM:H90.3 MIM:607821
Synonyms	autosomal recessive deafness 37 [EXACT] DFNB37 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness