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Metadata
ID DOID:0110488
Name autosomal recessive nonsyndromic deafness 3
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 MYO15A gene on chromosome 17p11.
https://www.ncbi.nlm.nih.gov/pubmed/17851452
Xrefs

ICD10CM:H90.3

OMIM:600316

Synonyms

autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3 [EXACT]

DFNB3 [EXACT]

NRSD3 [EXACT]

Parent Relationships

is_a autosomal recessive nonsyndromic deafness

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