"An autoimmune disease that is characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has material_basis_in X-linked recessive mutation in the forkhead box P3 (FOXP3) gene on chromosome Xp11."^^ . "XLAAD"@en . "ICD10CM:E31.0"^^ . _:vb50942274 . "IDDM-secretory diarrhea syndrome"@en . . "immunodeficiency, polyendocrinopathy, and enteropathy, X-linked"@en . "DOID:0090110"^^ . _:vb50942273 . "Autoimmune enteropathy type 1"@en . "OMIM:304790"^^ . "disease_ontology"^^ . _:vb50942273 . _:vb50942274 . . "GARD:1850"^^ . "diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked"@en . "immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome"^^ . "diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea"@en . _:vb50942273 . "autoimmunity-immunodeficiency syndrome, X-linked"@en . _:vb50942274 . "XPID"@en . . "immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked"@en . "X-linked autoimmunity-allergic dysregulation syndrome"@en . _:vb50942274 . "IPEX"@en . _:vb50942274 . . _:vb50942273 . "ORDO:37042"^^ . _:vb50942273 . "DMSD"@en .