Autoimmune polyendocrinopathy

Definition

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 Antiphospholipid Syndrome, APS, autoimmune polyendocrine syndrome, autoimmune polyendocrine syndrome; polyglandular autoimmune syndrome, autoimmune polyendocrinopathy, autoimmune polyendocrinopathy syndrome, autoimmune polyglandular failure, autoimmune polyglandular syndrome, autoimmune polyglandular syndrome(s) — per MONDO

Also identified as

• DOID 14040 per MONDO
• ICD10CM E31.0 per MONDO
• ICD9 258.8 per MONDO
• NCIT C129726 per MONDO
• NCIT C84576 per MONDO
• Orphanet 282196 per MONDO
• SCTID 41864002 per MONDO
• UMLS C0085409 per MONDO

Affected Organs