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Autoimmune polyendocrinopathy

MONDO:0017278

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.

Also known as: APS, Antiphospholipid Syndrome, autoimmune polyendocrine syndrome, autoimmune polyendocrine syndrome; polyglandular autoimmune syndrome, autoimmune polyendocrinopathy, autoimmune polyendocrinopathy syndrome, autoimmune polyglandular failure, autoimmune polyglandular syndrome

46 clinical trials for this condition and its sub-types, 3 tagged with Autoimmune polyendocrinopathy itself.

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