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

Gå till den engelska sidan

Basal ganglia calcification, idiopathic, 6

MONDO:0014628

Any bilateral striopallidodentate calcinosis in which the cause of the disease is a mutation in the XPR1 gene.

Also known as: XPR1 bilateral striopallidodentate calcinosis, basal ganglia calcification, idiopathic, 6, basal ganglia calcification, idiopathic, type 6, bilateral striopallidodentate calcinosis caused by mutation in XPR1, IBGC6

0 clinical trials for this condition and its sub-types, 0 tagged with Basal ganglia calcification, idiopathic, 6 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.