ORPHA:1877
Muscular dystrophy-white matter spongiosis syndrome
inactive · moved to ORPHA:258Laminin subunit alpha 2-related congenital muscular dystrophy
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Laminin subunit alpha 2-related congenital muscular dystrophy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Muscular dystrophy-white matter spongiosis syndrome | |
| fr | Syndrome de dystrophie musculaire-substance blanche cérébrale spongieuse | |
| de | Muskeldystrophie - Spongiosis der weissen Gehirnmasse | |
| es | Síndrome de distrofia muscular-espongiosis de la sustancia blanca | |
| it | Sindrome da distrofia muscolare e spongiosi della sostanza bianca | |
| nl | Spierdystrofie - spongiose van witte stof-syndroom | |
| pt | Síndrome de distrofia muscular-espongiose da substância branca | |
| pl | Dystrofia mięśni - zwyrodnienie gąbczaste istoty białej | |
| cs | Syndrom zahrnující svalovou dystrofii a spongiózu bílé hmoty | |
| uk | Синдром мязової дистрофії - спонгіозу білої речовини | |
| zh | 肌营养不良-白质海绵状硬化综合征 | |
| tr | Kas distrofisi-beyaz cevher spongioz sendromu |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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.
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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/1877
- This record as JSON: /data/d/1877.json