Addison disease
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Classic Addison' s disease Autoimmune Addison' s disease Primary Addison' s disease Autoimmune adrenalitis |
| Number of Symptoms | 4 |
| OrphanetNr: | 85138 |
| OMIM Id: |
103230
240200 |
| ICD-10: |
E27.1 |
| UMLs: |
C0001403 C0271737 |
| MeSH: |
D000224 |
| MedDRA: |
10001130 |
| Snomed: |
363732003 76715008 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
|
| Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Acquired chronic primary adrenal insufficiency
-Rare endocrine disease |
Symptom Information:
|
|
(HPO:0012605) | Hypernatriuria | 6 / 7739 | ||||
|
|
(HPO:0000846) | Adrenal insufficiency | 24 / 7739 | ||||
|
|
(HPO:0000953) | Hyperpigmentation of the skin | 75 / 7739 | ||||
|
|
(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|