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Metadata
ID DOID:0110535
Name autosomal recessive nonsyndromic deafness 9
Definition An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOF gene on chromosome 2p23.
https://www.ncbi.nlm.nih.gov/pubmed/10192385
Xrefs

ICD10CM:H90.3

MIM:601071

Synonyms

autosomal recessive deafness 9 [EXACT]

DFNB9 [EXACT]

neurosensory nonsyndromic recessive deafness 9 [EXACT]

NRSD9 [EXACT]

Parent Relationships

is_a autosomal recessive nonsyndromic deafness

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