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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: autosomal recessive deafness 28, DFNB28
Xenbase Genes : triobp
MONDO:0012355 - autosomal recessive nonsyndromic hearing loss 28 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee