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Metadata
ID DOID:0110544
Name autosomal dominant nonsyndromic deafness 12
Definition An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.
https://www.ncbi.nlm.nih.gov/pubmed/9590290
Xrefs

ICD10CM:H90.3

OMIM:601543

Synonyms

autosomal dominant deafness 12 [EXACT]

autosomal dominant deafness 8 [EXACT]

DFNA12 [EXACT]

DFNA8 [EXACT]

Parent Relationships

is_a autosomal dominant nonsyndromic deafness

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