ORPHA:264
Autosomal dominant limb-girdle muscular dystrophy type 1B
inactive · moved to ORPHA:98853Autosomal dominant Emery-Dreifuss muscular dystrophy
Synonyms: LGMD1B · Limb-girdle muscular dystrophy due to lamin A/C deficiency
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Autosomal dominant Emery-Dreifuss muscular dystrophy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Autosomal dominant limb-girdle muscular dystrophy type 1B | LGMD1B · Limb-girdle muscular dystrophy due to lamin A/C deficiency |
| fr | Dystrophie musculaire des ceintures autosomique dominante type 1B | Dystrophie musculaire des ceintures par déficit en lamine A/C · LGMD1B |
| de | Gliedergürtelmuskeldystrophie, autosomal-dominante, Typ 1B | Gliedergürtelmuskeldystrophie durch Lamin A/C -Mangel · LGMD1B |
| es | Distrofia muscular de cinturas autosómica dominante tipo 1B | Distrofia muscular de cinturas por deficiencia de lamina A/C · LGMD1B |
| it | Distrofia muscolare dei cingoli, autosomica dominante, tipo 1B | Distrofia muscolare dei cingoli da deficit di lamina A/C · LGMD1B |
| nl | Autosomaal dominante limb-girdle-spierdystrofie type 1B | Autosomaal dominante ledemaatgordel-spierdystrofie type 1B · LGMD1B · Limb-girdle-spierdystrofie door lamine A/C-deficiëntie · Autosomaal dominante bekken- en schoudergordel-spierdystrofie type 1B |
| pt | Distrofia muscular das cinturas dos membros autossómica dominante tipo 1B | Distrofia muscular das cinturas dos membros por deficiência de lamina A/C |
| pl | Autosomalna recesywna dystrofia obręczowo-kończynowa typu 1B | Dystrofia obręczowo-kończynowa z powodu niedoboru laminy A/C · LGMD1B |
| cs | Autozomálně dominantní pletencová svalová dystrofie, typ 1B | LGMD1B · Pletencová svalová dystrofie způsobená deficitem laminu A/C |
| uk | Аутосомно-домінантна мязова дистрофія скелетних мязів кінцівок, тип 1B | LGMD1B · Мязова дистрофія мязів поясу кінцівок внаслідок дефіциту ламіну А/С |
| zh | 1B型常染色体显性遗传肢带肌营养不良 | LGMD1B |
| tr | Otozomal dominant ekstremite kavşak tip kas distrofisi tip 1B | Lamin A / C eksikliğine bağlı ekstremite-kavşak tipi kas distrofisi · LGMD1B |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C1834653 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/264
- This record as JSON: /data/d/264.json