Autoimmune polyendocrinopathy type 2

Preferred Label : Autoimmune polyendocrinopathy type 2;

ICD-11 definition : This is the most common form of the polyglandular failure syndromes. It is more heterogeneous and has not been linked to one gene. Rather, patients are at a higher risk when they carry a particular human leukocyte antigen genotype (DQ2, DQ8 and DRB1*0404). APS-II affects women to a greater degree than men (75% of cases occur in women).;

ICD-11 synonym : Autoimmune thyroid disease and/or type 1 diabetes - Addison disease; Autoimmune polyglandular syndrome type 2; APS type 2- [autoimmune polyendocrine syndrome type 2]; Schmidt syndrome; APS type 2; autoimmune polyendocrine syndrome type 2;

Details

Origin ID

1065249344;

Automatic exact mappings (from CISMeF team)
- A. Schmidt's syndrome (disorder) [SNOMED CT concept]
- Autoimmune polyglandular failure [ICD-10 Sub-category]
- a. schmidt's syndrome [SNOMED Notion]
- polyendocrinopathies, autoimmune [MeSH Descriptor]
Currated CISMeF NLP mapping
- Autoimmune Polyglandular Syndrome Type 2 [NCIt concept]
- Autoimmune polyendocrine syndrome type II [MedDRA LLT]
- Autoimmune polyendocrine syndrome, type II [OMIM Phenotype]
- Autoimmune polyendocrinopathy type 2 [ORDO Disease]
- Polyglandular autoimmune syndrome, type 2 (disorder) [SNOMED CT concept]
- Schmidt's syndrome [MedDRA LLT]
- autoimmune polyendocrine syndrome type 2 [DO Concept]
- polyglandular autoimmune syndrome, type 2 [SNOMED Notion]
- polyglandular type II autoimmune syndrome [MeSH concept]

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