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Metadata
ID DOID:0110576
Name autosomal dominant nonsyndromic deafness 50
Definition An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has_material_basis_in mutation in the MIRN96 gene on chromosome 7q32.
https://www.ncbi.nlm.nih.gov/pubmed/19363479
Xrefs

ICD10CM:H90.3

OMIM:613074

Synonyms

autosomal dominant deafness 50 [EXACT]

DFNA50 [EXACT]

Parent Relationships

is_a autosomal dominant nonsyndromic deafness

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