Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7

MONDO:0013835

Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the ISPD gene.

Also known as: ISPD muscular dystrophy-dystroglycanopathy, type A, Walker-Warburg syndrome or muscle-eye-brain disease, ISPD-related, muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7, muscular dystrophy-dystroglycanopathy, type A caused by mutation in ISPD, MDDGA7

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

Follow this condition — get notified about new trials

Broader categories

Sort by