ORPHA:2033
OBSOLETE: Multifocal muscular fibrosis-obstructed vessels syndrome
inactive · referred to ORPHA:98006Rare neurologic disease
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare neurologic disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Multifocal muscular fibrosis-obstructed vessels syndrome | |
| fr | OBSOLETE : Syndrome de fibrose musculaire multifocale-vaisseaux obstrués | |
| de | OBSOLET: Muskelfibrose, multifokale, mit Gefässverschluss | |
| es | OBSOLETO: Síndrome de fibrosis muscular multifocal-vasos obstruidos | |
| it | OBSOLETO: Fibrosi muscolare multifocale - ostruzione dei vasi | |
| nl | OBSOLEET: Multifocale spierfibrose - verstopte bloedvaten-syndroom | |
| pt | OBSOLETO: Síndrome de fibrose muscular multifocal-oclusão dos vasos | |
| pl | NIEAKTUALNE: Wieloogniskowe wlóknienie miesni - zwezenie naczyn | |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující multifokální svalovou fibrózu a obstrukci cév | |
| uk | ЗАСТАРІЛО: Синдром мультифокального мязевого фіброзу-обструкції судин | |
| zh | 弃用:多灶性肌肉纤维化-血管阻塞综合征 | |
| tr | Eski adı: Multifokal musküler fibroz ile tıkalı damar sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/2033
- This record as JSON: /data/d/2033.json