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Metadata
DOID DOID:0110511
Name autosomal recessive nonsyndromic deafness 59
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 DFNB59 gene on chromosome 2q31.
https://www.ncbi.nlm.nih.gov/pubmed/17301963
Synonyms

autosomal recessive deafness 59 [EXACT]

DFNB59 [EXACT]

Xrefs

ICD10CM:H90.3

OMIM:610220

Relationships

is_a autosomal recessive nonsyndromic deafness

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