OMOP Concept 4008545

Polyglandular autoimmune syndrome, type 1

StandardConditionSNOMED11244009Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

4 source codes normalize to Polyglandular autoimmune syndrome, type 1 via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Polyglandular autoimmune syndrome, type 1 across source vocabularies.

  • APECED - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
  • Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
  • Autoimmune polyendocrinopathy, candidosis AND ectodermal dystrophy
  • Candidiasis-endocrinopathy syndrome
  • déficit poliglandular asociado con candidiasis mucocutánea
  • HAM syndrome
  • hipoparatiroidismo, enfermedad de Addison Y moniliasis
  • Hypoadrenocorticism, hypoparathyroidism and superficial moniliasis
  • Hypoparathyroidism, Addison's disease AND moniliasis
  • Juvenile familial endocrinopathy
  • Polyglandular autoimmune syndrome - type 1
  • Polyglandular autoimmune syndrome, type 1 (disorder)
  • Polyglandular deficiency associated with mucocutaneous candidiasis
  • síndrome de Whitaker
  • síndrome poliglandular autoinmunitario, tipo 1
  • síndrome poliglandular autoinmunitario, tipo 1 (trastorno)
  • Type 1 polyendocrine autoimmunity syndrome
  • Whitaker syndrome

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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