autosomal dominant nonsyndromic deafness 67

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Summary

Literature (0)

DOID:0110588 - autosomal dominant nonsyndromic deafness 67

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the OSBPL2 gene on chromosome 20q13.

Synonyms: DFNA67, autosomal dominant deafness 67,

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

: osbpl2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014594 - autosomal dominant nonsyndromic hearing loss 67

MONDO:0014594 - autosomal dominant nonsyndromic hearing loss 67

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

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

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