Telangiectasia, hereditary hemorrhagic, type 2

MONDO:0010880

Any hereditary hemorrhagic telangiectasia in which the cause of the disease is a mutation in the ACVRL1 gene.

Also known as: ACVRL1 hereditary hemorrhagic telangiectasia, hereditary hemorrhagic telangiectasia caused by mutation in ACVRL1, telangiectasia, hereditary hemorrhagic, type 2, HHT2, ORW2, Osler Weber Rendu syndrome type 2, hereditary hemorrhagic telangiectasia type 2, pulmonary arterial hypertension, hereditary hemorrhagic telangiectasia-related

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

Follow this condition — get notified about new trials

Broader categories

Sort by