Visualize Submit Comment
Metadata
ID DOID:0110526
Name autosomal recessive nonsyndromic deafness 79
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 TPRN gene on chromosome 9q34.
https://www.ncbi.nlm.nih.gov/pubmed/20170899
Xrefs

ICD10CM:H90.3

MIM:613307

Synonyms

autosomal recessive deafness 79 [EXACT]

DFNB79 [EXACT]

Parent Relationships

is_a autosomal recessive nonsyndromic deafness

Add an item to the term tracker