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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 : osbpl2

Mondo Disease Ontology (on Monarch Initiative):
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)