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Summary Literature (0)
DOID:0110526 - autosomal recessive nonsyndromic deafness 79

Disease Ontology 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.

Synonyms: DFNB79, autosomal recessive deafness 79,

Xenbase Genes : tprn

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013215 - autosomal recessive nonsyndromic hearing loss 79

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive nonsyndromic deafness (is_a)