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

Echinobase Genes :


OMIM:

MIM:601072 - deafness, autosomal recessive 8; dfnb8

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

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