ORPHA:206656
Non-dystrophic 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 | Non-dystrophic myopathy | |
| fr | Myopathies non dystrophiques | |
| de | Myopathie, nichtdystrophe | |
| es | Miopatía no distrófica | |
| it | Miopatia non distrofica | |
| nl | Niet-dystrofische myopathie | |
| pt | Miopatia não-distrófica | |
| pl | Miopatia niedystroficzna | |
| cs | Nedystrofická myopatie | |
| uk | Недистрофічна міопатія | |
| zh | 非营养不良性肌病 | |
| tr | Distrofik olmayan miyopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16110 | E | validated | |
| UMLS | C5680802 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:206634Genetic skeletal muscle disease
rare genetic diseases; rare neurological diseases
Children (15):
- ORPHA:689021Asymptomatic hyperCKemia-myalgia-rhabdomyolysis syndrome
- ORPHA:53347Brody myopathy
- ORPHA:97245Congenital myopathy
- ORPHA:289377Early-onset myopathy with fatal cardiomyopathy
- ORPHA:972Hereditary continuous muscle fiber activity
- ORPHA:221043Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome
- ORPHA:206662Inclusion myopathy
- ORPHA:98486Metabolic myopathy
- ORPHA:715623Motor incoordination-myopathy-respiratory insufficiency-progressive cerebellar atrophy syndrome
- ORPHA:593Myofibrillar myopathy
- ORPHA:289380Myosclerosis
- ORPHA:607Nemaline myopathy
- ORPHA:401768Proximal myopathy with extrapyramidal signs
- ORPHA:521305Proximal myopathy with focal depletion of mitochondria
- ORPHA:97238Rippling muscle disease
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/206656
- This record as JSON: /data/d/206656.json