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

Gå till den engelska sidan

Cerebral cavernous malformation 2

MONDO:0011304

Any familial cerebral cavernous malformation in which the cause of the disease is a mutation in the CCM2 gene.

Also known as: CCM2, CCM2 familial cerebral cavernous malformation, cerebral cavernous malformation 2, cerebral cavernous malformation type 2, cerebral cavernous malformations type 2, cerebral cavernous malformations-2, familial cerebral cavernous malformation caused by mutation in CCM2, cerebral cavernous malformations 2

0 clinical trials for this condition and its sub-types, 0 tagged with Cerebral cavernous malformation 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.