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Metadata
ID	DOID:0110490
Name	autosomal recessive nonsyndromic deafness 31
Definition	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32. https://www.ncbi.nlm.nih.gov/pubmed/12833159
Xrefs	ICD10CM:H90.3 OMIM:607084
Synonyms	autosomal recessive deafness 31 [EXACT] DFNB31 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness