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Metadata
ID	DOID:0110479
Name	autosomal recessive nonsyndromic deafness 21
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 TECTA gene on chromosome 11q23.3. https://www.ncbi.nlm.nih.gov/pubmed/9949200
Xrefs	ICD10CM:H90.3 MIM:603629
Synonyms	autosomal recessive deafness 21 [EXACT] DFNB21 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness