Complement component 7 deficiency
MONDO:0012412Any classic complement early component deficiency in which the cause of the disease is a mutation in the C7 gene.
Also known as: C7 classic complement early component deficiency, classic complement early component deficiency caused by mutation in C7, complement component 7 deficiency, C7 deficiency, C7D
41 clinical trials for this condition and its sub-types, 0 tagged with Complement component 7 deficiency itself.
Follow this condition to get notified about new trialsWhere 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.