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Metadata
ID	DOID:0110518
Name	autosomal recessive nonsyndromic deafness 67
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 LHFPL5 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/16459341
Xrefs	ICD10CM:H90.3 MIM:610265
Synonyms	autosomal recessive deafness 67 [EXACT] DFNB67 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness