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Summary Literature (0)
DOID:0050759 - myotonic dystrophy type 2

Disease Ontology Definition:A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_material_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one.

Synonyms: proximal myotonic myopathy

Xenbase Genes : cnbp

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011266 - myotonic dystrophy type 2

MIM:
MIM:602668 - MYOTONIC DYSTROPHY 2; DM2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): myotonic disease (is_a)