(Q3508566)

English

immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome

hypersensitivity reaction type II disease characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has material basis in mutation in the FOXP3 gene on chromosome Xp11

  • DMSD
  • diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea
  • autoimmunity-immunodeficiency syndrome, X-linked
  • immunodeficiency, polyendocrinopathy, and enteropathy, X-linked
  • diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked
  • XLAAD
  • XPID
  • IDDM-secretory diarrhea syndrome
  • IPEX
  • X-linked autoimmunity-allergic dysregulation syndrome
  • immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked
  • Autoimmune enteropathy type 1
  • Enteropathy, Autoimmune, With Hemolytic Anemia and Polyendocrinopathy
  • Immune Dysfunction and Diarrhea Syndrome
  • Immune Dysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome
  • Polyendocrinopathy, Immune Dysfunction, and Diarrhea, X-Linked
  • X linked Polyendocrinopathy
  • Islets of Langerhans, Absence of
  • IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX
  • Immunodeficiency, Polyendocrinopathy, and Enteropathy, X-Linked, Formerly

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