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Metadata
ID	DOID:0110526
Name	autosomal recessive nonsyndromic deafness 79
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 TPRN gene on chromosome 9q34. https://www.ncbi.nlm.nih.gov/pubmed/20170899
Xrefs	ICD10CM:H90.3 OMIM:613307
Synonyms	autosomal recessive deafness 79 [EXACT] DFNB79 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness