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autoimmune polyendocrine syndrome type 1

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

Autoimmune polyendocrinopathy type 1, or APECED syndrome, is a genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure.

Synonyms

  • AIRE autoimmune polyendocrinopathy
  • APECED syndrome
  • APS 1
  • APS type 1
  • APS1
  • Autoimmune Polyglandular Syndrome Type 1
  • MEDAC syndrome
  • PGA 1
  • Whitaker syndrom
  • Whitaker syndrome
  • aire autoimmune polyendocrinopathy
  • autoimmune hypoparathyroidism-chronic candidiasis-Addison disease syndrome
  • autoimmune polyendocrine syndrome type 1
  • autoimmune polyendocrine syndrome, type I, with or without reversible metaphyseal dysplasia
  • autoimmune polyendocrinopathy caused by mutation in AIRE
  • autoimmune polyendocrinopathy caused by mutation in aire
  • autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia
  • autoimmune polyendocrinopathy syndrome type 1
  • autoimmune polyendocrinopathy syndrome, type I, autosomal dominant
  • autoimmune polyendocrinopathy type 1
  • autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
  • autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)
  • autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome
  • autoimmune polyglandular syndrome I
  • autoimmune polyglandular syndrome type 1
  • autoimmune polyglandular syndrome, type 1
  • ham syndrome
  • hypoadrenocorticism with hypoparathyroidism and superficial Moniliasis
  • hypoparathyroidism-Addison disease-mucocutaneous candidiasis syndrome
  • multiple endocrine deficiency-Addison disease-candidiasis syndrome
  • polyglandular autoimmune syndrome type 1
  • polyglandular autoimmune syndrome, type 1
  • polyglandular deficiency syndrome, Persian-Jewish type
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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