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DOID:0110281 - autosomal recessive limb-girdle muscular dystrophy type 2G
Disease Ontology Definition:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the gene encoding telethonin (TCAP).
Synonyms: LGMD2G, limb-girdle muscular dystrophy due to telethonin deficiency, muscular dystrophy, limb-girdle, type 2G,
Echinobase Genes :
MIM:601954 - muscular dystrophy, limb-girdle, type 2g; lgmd2g |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee