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Summary Literature (0)
DOID:0110477 - autosomal recessive nonsyndromic deafness 2


Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.

Synonyms: DFNB2, autosomal recessive deafness 2

Xenbase Genes : myo7a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010807 - autosomal recessive nonsyndromic deafness 2

OMIM:
OMIM:600060 - DEAFNESS, AUTOSOMAL RECESSIVE 2; DFNB2

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)