{"diseases":[{"id":"ORPHA:228426","name":"Syndromic multisystem autoimmune disease due to Itch deficiency","mondoId":"MONDO:0013245","description":null},{"id":"ORPHA:37042","name":"Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome","mondoId":"MONDO:0010580","description":null}],"genes":[{"id":"NCBIGene:83737","name":"ITCH"},{"id":"NCBIGene:50943","name":"FOXP3"}],"assays":[],"medicalActions":[]}