Type I complement component 8 deficiency
MONDO:0013422Any 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.
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