Cure My Disease

Don't miss your cure!

 Log in / Sign up

Myopathy caused by variation in GMPPB

MONDO:0700084

Any myopathy in which the cause of the disease is a variation in the GMPPB gene.

Also known as: GMPPB-related myopathy, myopathy caused by mutation in GMPPB

62 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Sub-types

Autosomal recessive limb-girdle muscular dystrophy type 2T (1) Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14 (0) Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14 (0)

Broader categories

Disease (618) Nervous system disorder (217) Metabolic disease (215) Musculoskeletal system disorder (196) Hereditary disease (172) Muscle tissue disorder (53) Inborn errors of metabolism (42) Human disease (14) Myopathy (11) Skeletal muscle disorder (8)
Trials to join now! 32 Not yet recruiting 9 Not yet finished but already full! 7 Completed 13 Terminated 1
Sort by