autosomal recessive nonsyndromic deafness 18B

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Summary

Literature (0)

DOID:0110474 - autosomal recessive nonsyndromic deafness 18B

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the OTOG gene on chromosome 11p15.

Synonyms: DFNB18B, autosomal recessive deafness 18B,

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

: otog

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013985 - autosomal recessive nonsyndromic hearing loss 18B

MONDO:0013985 - autosomal recessive nonsyndromic hearing loss 18B

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

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

Parent(s): autosomal recessive nonsyndromic deafness (is_a)