ORPHA:645617
Amyopathic dermatomyositis
Synonyms: Dermatomyositis sine myositis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Amyopathic dermatomyositis | Dermatomyositis sine myositis |
| fr | Dermatomyosite amyopathique | Dermatomyosite sine myositis |
| de | Dermatomyositis, amyopathische | Dermatomyositis ohne Myositis |
| es | Dermatomiositis amiopática | Dermatomiositis sin miositis |
| it | Dermatomiosite amiopatica | Dermatomiosite senza miosite |
| nl | Amyopathische dermatomyositis | = en |
| pt | Dermatomiosite amiopática | Dermatomiosite sine miosite |
| pl | Amiopatyczne zapalenie skórno-mięśniowe | = en |
| cs | Amyopatická dermatomyozitida | = en |
| uk | Аміопатичний дерматоміозит | Дерматоміозит синус-міозит |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0043317 | E | validated | |
| MeSH | C538250 | E | validated | |
| UMLS | C0406645 | E | validated | |
| GARD | 9907 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/645617
- This record as JSON: /data/d/645617.json