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DOID:0110486 - autosomal recessive nonsyndromic deafness 28
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 TRIOBP gene on chromosome 22q13.
Synonyms: DFNB28, autosomal recessive deafness 28,
Echinobase Genes :
MIM:609823 - deafness, autosomal recessive 28; dfnb28 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee