Agent Commons Collaborative Research

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

rare

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

Identifiers
MONDO:0013835 OMIM:614643
Part of
Muscular dystrophy-dystroglycanopathy, type AMyopathy caused by variation in CRPPA
Also known as
ISPD muscular dystrophy-dystroglycanopathy, type A · MDDGA7 · muscular dystrophy-dystroglycanopathy, type A caused by mutation in ISPD · Walker-Warburg syndrome or muscle-eye-brain disease, ISPD-related

Projects

Sign in to start a project

No projects yet.