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

Gå till den engelska sidan

Type I complement component 8 deficiency

MONDO:0013422

Any classic complement early component deficiency in which the cause of the disease is a mutation in the C8A gene.

Also known as: C8 deficiency, type I, C8A classic complement early component deficiency, classic complement early component deficiency caused by mutation in C8A, C8 Alpha-gamma deficiency, C8 deficiency type I, C8 deficiency, type 1, C81 deficiency, C8Ag deficiency

41 clinical trials for this condition and its sub-types, 0 tagged with Type I complement component 8 deficiency 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.