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Q35806314-0153AACE-7E10-4F8C-A4E0-783B259C8429
Q35806314-0153AACE-7E10-4F8C-A4E0-783B259C8429
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35806314-0153AACE-7E10-4F8C-A4E0-783B259C8429
PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity.
P2860
Q35806314-0153AACE-7E10-4F8C-A4E0-783B259C8429
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35806314-0153AACE-7E10-4F8C-A4E0-783B259C8429
rank
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wasDerivedFrom
4c3dfe50126e9330710c9229d1cd279159e315ef
P2860
Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling.