ORPHA:71281
Rare 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare central nervous system and retinal vascular disease | |
| fr | Maladie vasculaire rare du système nerveux central et de la rétine | |
| de | ZNS- und Netzhautkrankheit, vaskuläre seltene | |
| es | Enfermedad rara del sistema nervioso central y vascular de la retina | |
| it | Malattia rara vascolare retinica e del sistema nervoso centrale | |
| nl | Zeldzame vasculaire aandoening van centraal zenuwstelsel en retina | |
| pt | Doença vascular do sistema nervoso central e da retina, rara | |
| pl | Rzadka choroba centralnego układu nerwowego i choroba naczyniowa siatkówki | |
| cs | Vzácná porucha centrálního nervového systému a cévní choroba sítnice | |
| uk | Рідкісні захворювання центральної нервової системи та судин сітківки | |
| zh | 罕见中枢神经系统和视网膜血管疾病 | |
| tr | Nadir merkezi sinir sistemi ve retinal damar hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 19110 | E | validated | |
| UMLS | C5681266 | 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:98006Rare neurologic disease
rare neurological diseases
Children (22):
- ORPHA:90065Acquired aneurysmal subarachnoid hemorrhage
- ORPHA:329217Cerebral sinovenous thrombosis
- ORPHA:447788Cerebral visual impairment
- 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:209943IRVAN syndrome
- ORPHA:689001Isolated spontaneous cervical artery dissection
- ORPHA:477768Moyamoya angiopathy
- ORPHA:404463Multisystemic smooth muscle dysfunction syndrome
- ORPHA:137577Neonatal hypoxic and ischemic brain injury
- ORPHA:102006Neurovascular malformation
- ORPHA:439175Pediatric arterial ischemic stroke
- ORPHA:140989Primary angiitis of the central nervous system
- ORPHA:758Pseudoxanthoma elasticum
- ORPHA:482092Rare idiopathic macular telangiectasia
- ORPHA:820Sneddon syndrome
- ORPHA:838Susac syndrome
- ORPHA:353356Vasoproliferative tumor of the retina
- 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/71281
- This record as JSON: /data/d/71281.json