centronuclear myopathy 2

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Summary

Literature (0)

DOID:0111220 - centronuclear myopathy 2

Disease Ontology Definition:An autosomal recessive centronuclear myopathy that has_material_basis_in homozygous or compound heterozygous mutation in BIN1 on 2q14.3.

Synonyms: CNM2

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

: bin1

MIM:

MIM:255200 - MYOPATHY, CENTRONUCLEAR, 2; CNM2

MIM:255200 - MYOPATHY, CENTRONUCLEAR, 2; CNM2

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

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

Parent(s): autosomal recessive centronuclear myopathy (is_a)