ORPHA:98473
Muscular dystrophy
- 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 | Muscular dystrophy | |
| fr | Dystrophie musculaire | |
| de | Muskeldystrophie | |
| es | Distrofia muscular | |
| it | Distrofia muscolare | |
| nl | Spierdystrofie | |
| pt | Distrofia muscular | |
| pl | Dystrofia mięśniowa | |
| cs | Svalové dystrofie | |
| uk | Мязова дистрофія | |
| zh | 肌营养不良 | |
| tr | Kas distrofisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | G71.0 | E | specific | validated |
| ICD-11 | 8C70 | E | specific | validated |
| MONDO | 0020121 | E | validated | |
| MeSH | D009136 | E | validated | |
| UMLS | C0026850 | E | validated | |
| GARD | 7922 | E | validated | |
| MedDRA | 10028356 | 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
Codes that Orphanet moved or referred to this one:
- ORPHA:2601OBSOLETE: Myopathy-growth delay-intellectual disability-hypospadias syndrome referred to · inactive
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/98473
- This record as JSON: /data/d/98473.json