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Metadata
ID	DOID:0110519
Name	autosomal recessive nonsyndromic deafness 68
Definition	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the S1PR2 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/26805784
Xrefs	ICD10CM:H90.3 OMIM:610419
Synonyms	autosomal recessive deafness 68 [EXACT] DFNB68 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness