Fungal myositis
- Type
- Disease
- Group
- Disorder
- Age of onset
- All ages
- Status
- active
A rare acquired skeletal muscle disease characterized by inflammation of a muscle due to infection with a fungus, usually occurring in an immunocompromised host. General symptoms are pain, tenderness, swelling, and/or weakness in the affected muscle. Most common causative agent are <i>Candida</i> species, with myositis developing in the setting of systemic candidiasis, typically as diffuse, multiple microabscesses. Other fungal pathogens potentially causing myositis are <i>Cryptococcus neoformans</i>, <i>Histoplasma capsulatum</i>, <i>Coccidioides</i> species, or <i>Aspergillus</i> species, among others.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fungal myositis | |
| fr | Myosite fongique | |
| de | Myositis bei Pilzerkrankungen | |
| es | Miositis fúngica | |
| it | Miosite fungina | |
| nl | Fungale myositis | |
| pt | Miosite fúngica | |
| pl | Grzybicze zapalenie mięśni | |
| cs | Mykotická myozitida | |
| uk | Грибковий міозит | |
| zh | 真菌性肌炎 | |
| tr | Mantar miyoziti |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M60.0 | NTBT | attributed | validated |
| ICD-11 | FB30 | NTBT | index | validated |
| MONDO | 0016130 | E | validated | |
| UMLS | C0410251 | E | validated | |
| MedDRA | 10086251 | 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:206988Infectious, fungal or parasitic myopathy
rare neurological 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/207000
- This record as JSON: /data/d/207000.json