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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

OMIM:603629

Synonyms

autosomal recessive deafness 21 [EXACT]

DFNB21 [EXACT]

Parent Relationships

is_a autosomal recessive nonsyndromic deafness

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