Familial mitral valve prolapse

MONDO:0008004

An instance of mitral valve prolapse (disease) that is caused by an inherited modification of the individual's genome.

Also known as: hereditary mitral valve prolapse (disease), MVP, mitral valve prolapse, familial, mitral valve prolapse, familial, autosomal dominant

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

Follow this condition — get notified about new trials

Sub-types

Broader categories

Sort by