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A20 haploinsufficiency

MONDO:0100222

Any immune dysregulation disease in which the cause of the disease is a mutation in the TNFAIP3 gene.

Also known as: HA20

42 clinical trials for this condition and its sub-types, 1 tagged with A20 haploinsufficiency itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary disease (18231) ↑ Inborn error of immunity (344)
Including sub-types (42) Tagged with A20 haploinsufficiency (1)
Trials to join now! 1
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