centronuclear myopathy X-linked

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

DOID:0111225 - centronuclear myopathy X-linked

Disease Ontology Definition:A centronuclear myopathy that has_material_basis_in X-linked inheritance of mutations in MTM1 on Xq28.

Synonyms: CNMX, MTM1, X-linked myotubular myopathy, XLCNM, XLMTM, myotubular myopathy 1,

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

: mtm1

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

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

Parent(s): centronuclear myopathy (is_a)