Autoimmune polyendocrinopathy

rare

A group of diverse conditions that are characterized by spontaneous, multi-organ autoimmunity, which target both endocrine (adrenal, gonad, pancreatic islet cells, parathyroid, pituitary, thyroid) and non-endocrine (gastrointestinal, integumentary, lymphatic) tissues.

Identifiers: MONDO:0017278 Orphanet:282196
Part of: Autoimmune disorder of endocrine system Polyendocrinopathy Syndromic disease
Also known as: APS · autoimmune polyendocrine syndrome · autoimmune polyendocrine syndrome; polyglandular autoimmune syndrome · autoimmune polyendocrinopathy syndrome · autoimmune polyglandular failure

Subtypes

All diseases Rare only

Disease	ID	Genes
Autoimmune polyendocrine syndrome type 1	MONDO:0009411	AIRE
Autoimmune polyendocrinopathy type 2	MONDO:0010012
Autoimmune polyendocrinopathy type 3	MONDO:0016422
Autoimmune polyendocrinopathy type 4	MONDO:0016423

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