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Muscular dystrophy-dystroglycanopathy, type C

rare

Identifiers: MONDO:0000173
Part of: Hereditary neuromuscular disease Hereditary skeletal muscle disorder Muscular dystrophy-dystroglycanopathy

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Autosomal recessive limb-girdle muscular dystrophy type 2I	MONDO:0011787
Autosomal recessive limb-girdle muscular dystrophy type 2K	MONDO:0012248
Autosomal recessive limb-girdle muscular dystrophy type 2M	MONDO:0012699
Autosomal recessive limb-girdle muscular dystrophy type 2N	MONDO:0013162
Autosomal recessive limb-girdle muscular dystrophy type 2O	MONDO:0013161
Autosomal recessive limb-girdle muscular dystrophy type 2P	MONDO:0013440		DAG1
Autosomal recessive limb-girdle muscular dystrophy type 2T	MONDO:0014142
Autosomal recessive limb-girdle muscular dystrophy type 2U	MONDO:0014474
Limb-girdle muscular dystrophy due to POMK deficiency	MONDO:0014489		POMK
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8	MONDO:0029135

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