Summary Literature (0)

DOID:0110527 - autosomal recessive nonsyndromic deafness 8

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TMPRSS3 gene on chromosome 21q22.

Synonyms: autosomal recessive deafness 10, autosomal recessive deafness 8, childhood-onset neurosensory autosomal recessive deafness 8, DFNB10, DFNB8, neurosensory nonsyndromic recessive deafness 8, NRSD8

Xenbase Genes : tmprss3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010987 - autosomal recessive nonsyndromic hearing loss 8

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee