ORPHA:206662
Inclusion myopathy
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Inclusion myopathy | |
| fr | Myopathie à inclusion | |
| de | Einschlusskörper-Myopathie | |
| es | Miopatía por cuerpos de inclusión | |
| it | Miopatia da inclusione | |
| nl | Inclusielichaammyopathie | |
| pt | Miopatia de inclusão | |
| pl | Miopatia wtrętowa | |
| cs | Myopatie s inkluzními tělísky | |
| uk | Міопатія з тільцями-включеннями | |
| zh | 包涵体肌病 | |
| tr | İnklüzyon miyopatisi |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16112 | E | validated | |
| UMLS | C5680794 | 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:206656Non-dystrophic myopathy
rare genetic diseases; rare neurological diseases
Children (9):
- ORPHA:363677Childhood-onset autosomal recessive myopathy with external ophthalmoplegia
- ORPHA:84132Desmin-related myopathy with Mallory body-like inclusions
- ORPHA:98909Desminopathy
- ORPHA:602GNE myopathy
- ORPHA:324381Hereditary inclusion body myopathy type 4
- ORPHA:79091Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
- ORPHA:178464Hereditary myopathy with early respiratory failure
- ORPHA:52430Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
- ORPHA:25980X-linked myopathy with excessive autophagy
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/206662
- This record as JSON: /data/d/206662.json