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

44 clinical trials for this condition and its sub-types, 0 tagged with Familial mitral valve prolapse itself.

Where it sits in the disease tree

Part of

Sub-types of Familial mitral valve prolapse

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