Autoimmune polyendocrinopathy
MONDO:0017278A 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.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of Autoimmune polyendocrinopathy
-
Autoimmune polyendocrinopathy type 4 0 trials