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Metadata
ID	DOID:0110494
Name	autosomal recessive nonsyndromic deafness 36
Definition	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/15286153
Xrefs	ICD10CM:H90.3 OMIM:609006
Synonyms	autosomal recessive deafness 36 [EXACT] DFNB36 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness