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MIM:617718 - IMMUNODEFICIENCY 71 WITH INFLAMMATORY DISEASE AND CONGENITAL THROMBOCYTOPENIA; IMD71
Xenbase Genes: arpc1b
Human Disease Resource: OMIM
MONDO:0060583 - platelet abnormalities with eosinophilia and immune-mediated inflammatory disease |
DOID:0112004 - immunodeficiency 71 |