Term Name:	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
Synonyms:	Autoimmune enteropathy type 1, autoimmunity-immunodeficiency syndrome, X-linked, diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea, diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked, DMSD, IDDM-secretory diarrhea syndrome, immunodeficiency, polyendocrinopathy, and enteropathy, X-linked, immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked, IPEX, X-linked autoimmunity-allergic dysregulation syndrome, XLAAD, XPID
Definition:	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.
Ontology:	Human Disease [DOID:0090110]   ( DOID:0090110 )