ORPHA:371436
Genetic neurovascular malformation
- 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 | Genetic neurovascular malformation | |
| fr | Malformation neurovasculaire d'origine génétique | |
| de | Neurovaskuläre Fehlbildung, genetisch bedingte | |
| es | Malformación neurovascular genética | |
| it | Malformazione neurovascolare genetica | |
| nl | Genetische neurovasculaire malformatie | |
| pt | Malformação neurovascular genética | |
| pl | Malformacja nerwowo-naczyniowa uwarunkowana genetycznie | |
| cs | Geneticky podmíněné neurovaskulární malformace | |
| uk | Генетично обумовлена нейросудинна вада розвитку | |
| zh | 遗传性神经血管畸形 | |
| tr | Genetik nörovasküler malformasyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681150 | 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:183503Genetic central nervous system and retinal vascular disease
rare genetic diseases
Children (10):
- ORPHA:46724Brain arteriovenous malformation, nidus type
- ORPHA:221061Familial cerebral cavernous malformation
- ORPHA:231160Familial cerebral saccular aneurysm
- ORPHA:83454Glomuvenous malformation
- ORPHA:774Hereditary hemorrhagic telangiectasia
- ORPHA:1062Hereditary neurocutaneous malformation
- ORPHA:521445Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome
- ORPHA:42775PHACE syndrome
- ORPHA:71213Retinal cavernous hemangioma
- ORPHA:1053Vein of Galen malformation
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/371436
- This record as JSON: /data/d/371436.json