Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
19474018 | Polyglandular autoimmune syndrome, type 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
19476016 | Polyglandular deficiency associated with mucocutaneous candidiasis | en | Synonym | Active | Case insensitive | SNOMED CT core |
19477013 | Hypoparathyroidism, Addison's disease AND moniliasis | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
19478015 | Autoimmune polyendocrinopathy, candidosis AND ectodermal dystrophy | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
19479011 | Candidiasis-endocrinopathy syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
19481013 | HAM syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
19483011 | Juvenile familial endocrinopathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
19484017 | Whitaker syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
372533015 | Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy | en | Synonym | Active | Case insensitive | SNOMED CT core |
372534014 | Polyglandular autoimmune syndrome - type 1 | en | Synonym | Active | Case insensitive | SNOMED CT core |
372535010 | Type 1 polyendocrine autoimmunity syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
372536011 | Hypoadrenocorticism, hypoparathyroidism and superficial moniliasis | en | Synonym | Active | Case insensitive | SNOMED CT core |
372537019 | APECED - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy | en | Synonym | Active | Case sensitive | SNOMED CT core |
640170013 | Polyglandular autoimmune syndrome, type 1 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4543087014 | A rare genetic disease that manifests in childhood or early adolescence with a combination of chronic mucocutaneous candidiasis, hypoparathyroidism and autoimmune adrenal failure. The first manifestation of the disease (usually candidiasis) occurs in childhood with other manifestations appearing progressively. The most common autoimmune endocrine involvement is hypoparathyroidism (79-96% of cases). Adrenal failure most often manifests with concurrent mineralocorticoid and glucocorticoid deficiency (78% of cases). The disease is caused by mutations of the AIRE gene (21q22.3) coding for the AIRE transcription factor, which is involved in immune tolerance mechanisms and contributes to the negative selection of autoreactive T lymphocytes in the thymus, lymph nodes and spleen. Transmission is autosomal recessive. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Disease caused by microorganism or bacterial toxin reference set
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set