Idiopathic eosinophilic myositis
Synonyms: Idiopathic eosinophilia-associated myopathy
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture , as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Idiopathic eosinophilic myositis | Idiopathic eosinophilia-associated myopathy |
| fr | Myosite éosinophile idiopathique | |
| de | Idiopathische eosinophile Myositis | Eosinophilie-assoziierte Myopathie, idiopathisch |
| es | Miositis eosinofílica idiopática | Miopatía asociada a eosinofilia idiopática |
| it | Miosite eosinofila idiopatica | |
| nl | Idiopathische eosinofiele myositis | Idiopathische myopathie geassocieerd met eosinofilie |
| pt | Miosite eosinofílica idiopática | |
| pl | Idiopatyczne eozynofilowe zapalenie mięśni | = en |
| cs | Idiopatická eosinofilní myozitida | = en |
| uk | Ідіопатичний еозинофільний міозит | Ідіопатична міопатія, повязана з еозинофілією |
| zh | 特发性嗜酸性肌炎 | 特发性嗜酸性肌病 |
| tr | İdiyopatik eozinofilik miyozit | İdiyopatik eozinofili-ilişkili miyopati |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M60.8 | NTBT | attributed | validated |
| MONDO | 0016610 | E | validated | |
| UMLS | C4755301 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98482Idiopathic inflammatory myopathy
rare neurological diseases; rare systemic and rheumatological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/247724
- This record as JSON: /data/d/247724.json