ORPHA:233655
Rare genetic vascular disease
- 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 | Rare genetic vascular disease | |
| fr | Maladie vasculaire génétique rare | |
| de | Gefäßkrankheit, seltene, genetisch bedingte | |
| es | Enfermedades vasculares genéticas raras | |
| it | Malattia vascolare genetica rara | |
| nl | Zeldzame genetische vasculaire ziekte | |
| pt | Doença vascular genética rara | |
| pl | Rzadka choroba naczyniowa uwarunkowana genetycznie | |
| cs | Vzácné genetické vaskulární onemocnění | |
| uk | Рідкісне генетично обумовлене захворювання судин | |
| zh | 罕见遗传性血管疾病 | |
| tr | Nadir genetik vasküler hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16517 | E | validated | |
| UMLS | C5680923 | 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 (2):
- ORPHA:496924Non-inflammatory vasculopathy
rare circulatory system diseases - ORPHA:98053Rare genetic disease
rare genetic diseases
Children (9):
- ORPHA:90349Autosomal recessive cutis laxa type 1
- ORPHA:404553Deficiency of adenosine deaminase 2
- ORPHA:86Familial abdominal aortic aneurysm
- ORPHA:51608Generalized arterial calcification of infancy
- ORPHA:289601Hereditary arterial and articular multiple calcification syndrome
- ORPHA:314718Lethal arteriopathy syndrome due to fibulin-4 deficiency
- ORPHA:285014Rare disease with thoracic aortic aneurysm and aortic dissection
- ORPHA:425120STING-associated vasculopathy with onset in infancy
- ORPHA:820Sneddon 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/233655
- This record as JSON: /data/d/233655.json