ORPHA:285014
Rare disease with thoracic aortic aneurysm and aortic dissection
- 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 | Rare disease with thoracic aortic aneurysm and aortic dissection | |
| fr | Maladie rare avec anévrisme et dissection de l'aorte thoracique | |
| de | Seltene Krankheit mit thorakalem Aortenaneurysma und Aortendissektion | |
| es | Enfermedad rara con aneurisma aórtico torácico y disección aórtica | |
| it | Malattia rara con aneurisma dell'aorta toracica e dissezione aortica | TAAD familiare |
| nl | Zeldzame ziekte met thoracaal aorta-aneurysma en aorta-dissectie | |
| pt | Aneurisma e disseção torácica familiar | |
| pl | Rzadkie choroby z tętniakiem aorty piersiowej i rozwarstwieniem aorty | |
| cs | Vzácná onemocnění s aneuryzmatem hrudní aorty a aortální disekcí | |
| uk | Рідкісне захворювання з аневризмою грудного відділу аорти та розшаруванням аорти | |
| zh | 合并胸主动脉瘤和主动脉夹层的罕见疾病 | |
| tr | Torasik aort anevrizması ve aort diseksiyonu ile seyreden nadir hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 17311 | E | validated | |
| UMLS | C5681014 | 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 (2):
- ORPHA:233655Rare genetic vascular disease
rare genetic diseases; rare circulatory system diseases - ORPHA:97962Rare surgical thoracic disease
rare surgical thoracic diseases
Children (11):
- ORPHA:284984Aneurysm-osteoarthritis syndrome
- ORPHA:3342Arterial tortuosity syndrome
- ORPHA:229Familial aortic dissection
- ORPHA:402075Familial bicuspid aortic valve
- ORPHA:91387Familial thoracic aortic aneurysm and aortic dissection
- ORPHA:60030Loeys-Dietz syndrome
- ORPHA:558Marfan syndrome
- ORPHA:404463Multisystemic smooth muscle dysfunction syndrome
- ORPHA:284979Neonatal Marfan syndrome
- ORPHA:286Vascular Ehlers-Danlos syndrome
- ORPHA:622925X-linked severe syndromic thoracic aortic aneurysm and dissection
Codes that Orphanet moved or referred to this one:
- ORPHA:1057OBSOLETE: Intracranial aneurysms-multiple congenital anomalies syndrome referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/285014
- This record as JSON: /data/d/285014.json