ORPHA:329888
Juvenile idiopathic inflammatory myopathy
Synonyms: JIIM
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Juvenile idiopathic inflammatory myopathy | JIIM |
| fr | Myopathie inflammatoire idiopathique juvénile | JIIM · MIIJ |
| de | Myopathie, idiopathische inflammatorische, juvenile Form | = en |
| es | Miopatía inflamatoria idiopática juvenil | = en |
| it | Miopatia infiammatoria idiopatica giovanile | = en |
| nl | Juveniele idiopathische inflammatoire myopathie | = en |
| pt | Miopatia inflamatória idiopática juvenil | |
| pl | Młodzieńcza idiopatyczna miopatia zapalna | = en |
| cs | Juvenilní idiopatická zánětlivá myopatie | = en |
| uk | Ювенільна ідіопатична запальна міопатія | = en |
| zh | 青少年特发性炎性肌病 | = en |
| tr | Juvenil idiyopatik inflamatuar miyopati | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018010 | E | validated | |
| MONDO | 18010 | E | validated | |
| UMLS | C5679857 | 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:98482Idiopathic inflammatory myopathy
rare neurological diseases; rare systemic and rheumatological diseases
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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/329888
- This record as JSON: /data/d/329888.json