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Metadata
ID	DOID:0110520
Name	autosomal recessive nonsyndromic deafness 7
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 TMC1 gene on chromosome 9q21. https://www.ncbi.nlm.nih.gov/pubmed/11850618
Xrefs	ICD10CM:H90.3 MIM:600974
Synonyms	autosomal recessive deafness 7 [EXACT] DFNB11 [EXACT] DFNB7 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness