Autoimmune polyendocrine syndrome type 1

MONDO:0009411

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.

Also known as: AIRE autoimmune polyendocrinopathy, APECED syndrome, APS type 1, APS1, Autoimmune Polyglandular Syndrome Type 1, MEDAC syndrome, Whitaker syndrom, aire autoimmune polyendocrinopathy

48 clinical trials for this condition and its sub-types, 8 tagged with Autoimmune polyendocrine syndrome type 1 itself.

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Where it sits in the disease tree

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Part of

↑ Adrenal gland disorder (352) ↑ Hereditary hypoparathyroidism (26) ↑ Autoimmune polyendocrinopathy (11) ↑ Autoimmune hypoparathyroidism (8)

Including sub-types (48) Tagged with Autoimmune polyendocrine syndrome type 1 (8)

Trials to join now! 4 Completed 3 Terminated 1

Yeast study in rare autoimmune disease terminated early

Knowledge-focused Stopped early

This study aimed to compare the types of Candida yeast found in patients with two forms of autoimmune polyendocrinopathy, a rare condition where the immune system attacks multiple glands. Researchers planned to collect samples from the mouth and urine of 7 participants to see how…

Sponsor: University Hospital, Lille • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:37 UTC

Autoimmune polyendocrine syndrome type 1

Where it sits in the disease tree

Yeast study in rare autoimmune disease terminated early