Cardiac Valvular Dysplasia, X-Linked (CVDPX)

Alias:

Xmvd

Filamin a-Related X-Linked Myxomatous Valvular Dysplasia

Flna-Related X-Linked Myxomatous Valvular Dysplasia

X-Linked Cardiac Valvular Dysplasia

Flna-Related Valvular Dystrophy

X-Linked Myxomatous Valvular Dystrophy

Congenital Valvular Heart Disease

Ehlers-Danlos Syndrome Type 5

Cvdpx

Cvd1

Filamin-a-Associated Myxomatous Mitral Valve Disease

Filamin-a-Related Myxomatous Mitral Valve Dystrophy

Dysplasia, Valvular, Cardiac, X-Linked, Type 1

Ehlers-Danlos Syndrome, Type V, Formerly

Myxomatous Valvular Dystrophy, X-Linked

Dystrophie Valvulaire Associee a Flna

Valvular Heart Disease, Congenital

X-Linked Ehlers-Danlos Syndrome

Ehlers-Danlos Syndrome, Type 5

Ehlers-Danlos Syndrome Type V

Eds5, Formerly

X-Linked Eds

Eds 5

Eds V

Eds5

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cardiac Valvular Dysplasia, X-Linked, also known as xmvd, is related to marfan syndrome and contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a. An important gene associated with Cardiac Valvular Dysplasia, X-Linked is FLNA (Filamin A). Affiliated tissues include heart and skin, and related phenotypes are inguinal hernia and umbilical hernia

Related ID：

MALACARDS：CRD017

OMIM：314400

MESH：C536197