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Type II complement component 8 deficiency

MONDO:0013421

Any classic complement early component deficiency in which the cause of the disease is a mutation in the C8B gene.

Also known as: C8 deficiency, type II, C8B classic complement early component deficiency, classic complement early component deficiency caused by mutation in C8B, C8 Beta deficiency, C8 deficiency type II, C8 deficiency, type 2, C8B deficiency, C8D2

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

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