ORPHA:477771
Rare disorder with a moyamoya angiopathy
- 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 disorder with a moyamoya angiopathy | |
| fr | Maladie rare avec angiopathie de Moyamoya | |
| de | Seltene Krankheit mit Moyamoya-Angiopathie | |
| es | Trastorno raro con angiopatía de moyamoya | |
| it | Malattia rara con agiopatia di moyamoya | |
| nl | Zeldzame stoornis met een moyamoya-angiopathie | |
| pt | Doença rara com angiopatia de Moyamoya | |
| pl | Zespół Moyamoya | |
| cs | Vzácné onemocnění s moyamoya angiopatií | |
| uk | Рідкісне захворювання з ангіопатією Моямоя | |
| zh | 罕见病合并烟雾病 | |
| tr | Moyamoya anjiyopatisi ile seyreden nadir bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18792 | E | validated | |
| UMLS | C5681260 | 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:183503Genetic central nervous system and retinal vascular disease
rare genetic diseases - ORPHA:477768Moyamoya angiopathy
rare neurological diseases
Children (13):
- ORPHA:51Aicardi-Goutières syndrome
- ORPHA:3071Costello syndrome
- ORPHA:870Down syndrome
- ORPHA:481662Familial Chilblain lupus
- ORPHA:2637Microcephalic osteodysplastic primordial dwarfism type II
- ORPHA:280679Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome
- ORPHA:401945Moyamoya disease with early-onset achalasia
- ORPHA:636Neurofibromatosis type 1
- ORPHA:648Noonan syndrome
- ORPHA:363972Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
- ORPHA:42775PHACE syndrome
- ORPHA:232Sickle cell anemia
- ORPHA:881Turner 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/477771
- This record as JSON: /data/d/477771.json