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Summary Literature (0)
DOID:0111216 - autosomal recessive centronuclear myopathy


Disease Ontology Definition:A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance.

Synonyms: AR-CNM

Xenbase Genes : bin1, map3k20



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Disease Hierarchy:Legend: is acentronuclear myopathy 6 with fiber-type disproportion (0)centronuclear myopathy 5 (0)centronuclear myopathy 2 (0)autosomal recessive centronuclear myopathy (0)This image is generated by www.xenbase.org. Please cite Xenbase in your publications.
Parent(s): autosomal recessive disease (is_a), centronuclear myopathy (is_a)