ORPHA:183503
Genetic central nervous system and retinal 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Genetic central nervous system and retinal vascular disease | |
| fr | Maladie vasculaire du système nerveux central et de la rétine de cause génétique | |
| de | ZNS-Fehlbildung und vaskuläre Netzhautkrankheit, genetisch bedingt | |
| es | Enfermedad vascular del sistema nervioso central y de la retina de origen genético. | |
| it | Malattia vascolare del sistema nervoso centrale e della retina di origine genetica | |
| nl | Genetische centraal zenuwstelsel en retinale vasculaire ziekte | |
| pt | Doença genética do sistema nervoso central e vascular retiniana | |
| pl | Choroba centralnego układu nerwowego i naczyń siatkówki uwarunkowana genetycznie | |
| cs | Geneticky podmíněná onemocnění cév centrálního nervového systému a sítnice | |
| uk | Генетично обумовлене захворювання центральної нервової системи та судин сітківки | |
| zh | 遗传性中枢神经系统和视网膜血管病 | |
| tr | Genetik merkezi sinir sistemi ve retina damar hastalığı |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15953 | E | validated | |
| UMLS | C5681839 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:71859Rare genetic neurological disorder
rare genetic diseases
Children (12):
- ORPHA:190Coats disease
- ORPHA:891Familial exudative vitreoretinopathy
- ORPHA:569Familial or sporadic hemiplegic migraine
- ORPHA:284247Familial retinal arterial macroaneurysm
- ORPHA:477754Genetic cerebral small vessel disease
- ORPHA:371436Genetic neurovascular malformation
- ORPHA:689001Isolated spontaneous cervical artery dissection
- ORPHA:404463Multisystemic smooth muscle dysfunction syndrome
- ORPHA:140989Primary angiitis of the central nervous system
- ORPHA:758Pseudoxanthoma elasticum
- ORPHA:477771Rare disorder with a moyamoya angiopathy
- ORPHA:892Von Hippel-Lindau disease
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/183503
- This record as JSON: /data/d/183503.json