ORPHA:102014
Autosomal dominant limb-girdle muscular dystrophy
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Autosomal dominant
- 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 | Autosomal dominant limb-girdle muscular dystrophy | |
| fr | Dystrophie musculaire des ceintures autosomique dominante | |
| de | Gliedergürtelmuskeldystrophie, autosomale-dominante | |
| es | Distrofia muscular de cinturas autosómica dominante | |
| it | Distrofia muscolare dei cingoli, autosomica dominante | |
| nl | Autosomaal dominante limb-girdle-spierdystrofie | Autosomaal dominante bekken- en schoudergordel-spierdystrofie · Autosomaal dominante ledemaatgordel-spierdystrofie |
| pt | Distrofia muscular das cinturas dos membros autossómica dominante | |
| pl | Autosomalana dominująca dystrofia obręczowo-kończynowa | |
| cs | Autozomálně dominantní svalové dystrofie končetinového pletence | |
| uk | Аутосомно-домінантна мязова дистрофія кінцівок і поясів | |
| zh | 常染色体显性遗传肢体带状肌营养不良 | |
| tr | Otozomal dominant ekstremite-kuşak kas distrofisi |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 8C70.40 | E | specific | validated |
| MONDO | 0015151 | E | validated | |
| MONDO | 15151 | E | validated | |
| UMLS | C5675009 | 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:263Limb-girdle muscular dystrophy
rare genetic diseases; rare neurological diseases
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/102014
- This record as JSON: /data/d/102014.json