ORPHA:645626
Adermatopathic dermatomyositis
Synonyms: Dermatomyositis sine dermatitis
- 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 | Adermatopathic dermatomyositis | Dermatomyositis sine dermatitis |
| fr | Dermatomyosite sine dermatitis | |
| de | Dermatomyositis, adermatopathische | Dermatomyositis ohne Dermatitis |
| es | Dermatomiositis adermatopática | Dermatomiositis sin dermatitis |
| it | Dermatomiosite adermopatica | Dermatomiosite senza dermatite |
| nl | Adermatopathische dermatomyositis | = en |
| pt | Dermatomiosite adermatopática | Dermatomiosite sine dermatite |
| pl | Adermatopatyczne zapalenie skórno-mięśniowe | = en |
| cs | Adermatopatická dermatomyozitida | = en |
| uk | Адерматопатичний дерматоміозит | Дерматоміозит синегнійний дерматит |
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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 | 0957458 | E | validated | |
| UMLS | C5816708 | 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.
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/645626
- This record as JSON: /data/d/645626.json