ORPHA:102006
Neurovascular malformation
- Type
- Category
- Group
- Group of disorders
- Age of onset
- All ages
- 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 | Neurovascular malformation | |
| fr | Malformation neurovasculaire | |
| de | Neurovaskuläre Fehlbildung | Neurovaskuläre Malformation |
| es | Malformación neurovascular | |
| it | Malformazione neurovascolare | |
| nl | Neurovasculaire malformatie | |
| pt | Malformação neurovascular | |
| pl | Malformacja nerwowo-naczyniowa | |
| cs | Neurovaskulární malformace | |
| uk | Нервово-судинні вади розвитку | |
| zh | 神经血管畸形 | |
| tr | Nörovasküler malformasyon |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15145 | E | validated | |
| UMLS | C5681774 | E | validated | |
| GARD | 19819 | 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:71281Rare central nervous system and retinal vascular disease
rare neurological diseases
Children (14):
- ORPHA:723432Central nervous system venous vascular malformation
- ORPHA:353334Congenital retinal arteriovenous communication
- ORPHA:231160Familial cerebral saccular aneurysm
- ORPHA:83454Glomuvenous malformation
- ORPHA:774Hereditary hemorrhagic telangiectasia
- ORPHA:1062Hereditary neurocutaneous malformation
- ORPHA:981Internal carotid absence
- ORPHA:715750Intracranial fast-flow vascular malformation
- ORPHA:715757Metameric fast-flow vascular malformation
- ORPHA:521445Microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome
- ORPHA:42775PHACE syndrome
- ORPHA:71213Retinal cavernous hemangioma
- ORPHA:715025Spinal fast-flow vascular malformation
- ORPHA:3205Sturge-Weber 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/102006
- This record as JSON: /data/d/102006.json