ORPHA:98894
Congenital muscular dystrophy type 1D
inactive · moved to ORPHA:370953Congenital muscular dystrophy due to dystroglycanopathy
Synonyms: MDC1D
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Congenital muscular dystrophy due to dystroglycanopathy
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital muscular dystrophy type 1D | MDC1D |
| fr | Dystrophie musculaire congénitale type 1D | CMD1D · DMC1D · MDC1D |
| de | Muskeldystrophie, kongenitale, Typ 1D | CMD1D · MDC1D |
| es | Distrofia muscular congénita tipo 1D | CMD1D |
| it | Distrofia muscolare congenita, tipo 1D | = en |
| nl | Congenitale spierdystrofie type 1D | CMD1D · MDC1D |
| pt | Distrofia muscular congénita, tipo 1d | |
| pl | Wrodzona dystrofia mięśniowa typu 1D | = en |
| cs | Vrozená svalová dystrofie, typ 1D | = en |
| uk | Вроджена мязова дистрофія, тип 1D | = en |
| zh | 先天性肌营养不良症ID型 | = en |
| tr | Doğumsal kas distrofisi tip 1D | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C1837229 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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/98894
- This record as JSON: /data/d/98894.json