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Metadata
DOID DOID:0110567
Name autosomal dominant nonsyndromic deafness 41
Definition An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in mutation in the P2RX2 gene on chromosome 12q24.
Synonyms

autosomal dominant deafness 41 [EXACT]

DFNA41 [EXACT]

Xrefs

ICD10CM:H90.3

OMIM:608224

Relationships

is_a autosomal dominant nonsyndromic deafness

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