immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome (Q3508566)

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A 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
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English
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
A 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

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