ORPHA:496924
Non-inflammatory vasculopathy
- Type
- Category
- Group
- Group of disorders
- 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 | Non-inflammatory vasculopathy | |
| fr | Vasculopathie non inflammatoire | |
| de | Vaskulopathie, non-inflammatorische | |
| es | Vasculopatía no inflamatoria | |
| it | Vasculopatia non infiammatoria | |
| nl | Niet-inflammatoire vasculopathie | |
| pt | Vasculopatia não inflamatória | |
| pl | Niezapalna waskulopatia | |
| cs | Nezánětlivá vaskulopatie | |
| uk | Незапальна васкулопатія | |
| zh | 非炎性血管病 | |
| tr | İnflamatuar olmayan vaskülopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681227 | 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:68362Rare vascular disease
rare circulatory system diseases
Children (16):
- ORPHA:90064Acute peripheral arterial occlusion
- ORPHA:1682Arterial dissection-lentiginosis syndrome
- ORPHA:280062Calciphylaxis
- ORPHA:698012Fibromuscular dysplasia
- ORPHA:723342Flow limitation in the iliac artery
- ORPHA:699068Fontan-associated liver disease
- ORPHA:689001Isolated spontaneous cervical artery dissection
- ORPHA:542643Livedoid vasculopathy
- ORPHA:675404May-Thurner syndrome
- ORPHA:641829Neonatal compartment syndrome
- ORPHA:439175Pediatric arterial ischemic stroke
- ORPHA:233655Rare genetic vascular disease
- ORPHA:529864Secondary erythromelalgia
- ORPHA:645350Segmental arterial mediolysis
- ORPHA:820Sneddon syndrome
- ORPHA:838Susac syndrome
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/496924
- This record as JSON: /data/d/496924.json