autosomal recessive limb-girdle muscular dystrophy type 2F

Summary

DOID:0110280 - autosomal recessive limb-girdle muscular dystrophy type 2F

Disease Ontology Definition:An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the sarcoglycan-delta gene (SGCD).

Synonyms: delta-sarcoglycanopathy, LGMD2F, limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency

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

: sgcd

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011028 - autosomal recessive limb-girdle muscular dystrophy type 2F

MONDO:0011028 - autosomal recessive limb-girdle muscular dystrophy type 2F

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

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

Parent(s): autosomal recessive limb-girdle muscular dystrophy (is_a)