ORPHA:645613
Classical dermatomyositis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Classical dermatomyositis | |
| fr | Dermatomyosite classique | |
| de | Dermatomyositis, klassische | |
| es | Dermatomiositis clásica | |
| it | Dermatomiosite classica | |
| nl | Klassieke dermatomyositis | |
| pt | Dermatomiosite clássica | |
| pl | Klasyczne zapalenie skórno-mięśniowe | |
| cs | Klasická dermatomyozitida | |
| uk | Класичний дерматоміозит |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M33.1 | NTBT | attributed | validated |
| ICD-11 | 4A41.0 | NTBT | attributed | validated |
| MONDO | 0957456 | E | validated | |
| UMLS | C5816707 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:221Dermatomyositis
rare neurological diseases; rare skin diseases; rare renal diseases; rare systemic and rheumatological diseases; rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/645613
- This record as JSON: /data/d/645613.json