Emery-Dreifuss muscular dystrophy 5, autosomal dominant

MONDO:0013072

Any autosomal dominant Emery-Dreifuss muscular dystrophy in which the cause of the disease is a mutation in the SYNE2 gene.

Also known as: Emery-Dreifuss muscular dystrophy 5, autosomal dominant, SYNE2 autosomal dominant Emery-Dreifuss muscular dystrophy, autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in SYNE2, EDMD5, EMERY-Dreifuss muscular dystrophy 5, autosomal dominant

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

Follow this condition — get notified about new trials

Broader categories

Sort by