autosomal recessive nonsyndromic deafness 93

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Summary

Literature (0)

DOID:0110537 - autosomal recessive nonsyndromic deafness 93

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the CABP2 gene on chromosome 11q13.

Synonyms: autosomal recessive deafness 93, DFNB93

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cabp2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013963 - autosomal recessive nonsyndromic hearing loss 93

MONDO:0013963 - autosomal recessive nonsyndromic hearing loss 93

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)