Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

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

5 clinical trials for this condition and its sub-types, 0 tagged with Telangiectasia, hereditary hemorrhagic, type 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by