Addisons disease diagnosis codes
Codelist metadata
- Coding system
- SNOMED CT (UK Clinical Edition)
- Coding system release
- 39.2.0
- Organisation
- NHSD Primary Care Domain Refsets
- Codelist ID
- nhsd-primary-care-domain-refsets/addisons_cod
- Version Tag
- 20241205
- Version ID
- 20fa485b
- Number of codes included
- 22
About
Description
Taken from the `ADDISONS_COD` refset published by NHSD. Contains public sector information licensed under the UK Open Government Licence v3.0 (https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 111562000 | Addison's disease |
| 11244009 | Polyglandular autoimmune syndrome, type 1 |
| 12427005 | Congenital primary adrenocortical hypofunction |
| 186270000 | Tuberculous Addison's disease |
| 237760008 | Addison's disease with adrenoleucodystrophy |
| 237828007 | Polyglandular autoimmune syndrome - type 1 |
| 297257004 | Glycerol kinase deficiency - contiguous gene syndrome |
| 34253008 | Myopathy in Addison's disease |
| 363732003 | Addison's disease |
| 367376006 | Addison's disease, NOS |
| 37495007 | Familial adrenocortical hypoplasia |
| 403252006 | Buccal pigmentation due to Addison's disease |
| 44685003 | Addison's disease due to tuberculosis |
| 45414006 | Glucocorticoid deficiency with achalasia |
| 65389002 | Adrenoleukodystrophy |
| 763311001 | Adrenomyodystrophy |
| 764960005 | Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency |
| 765326001 | Familial glucocorticoid deficiency |
| 76715008 | Addison's disease due to autoimmunity |
| 783092005 | 46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency |
| 78481000000105 | Addison's disease |
| 83728000 | Polyglandular autoimmune syndrome, type 2 |