ORPHA:494348
Early-onset familial noncirrhotic portal hypertension
inactive · moved to ORPHA:596937Portosinusoidal vascular disease
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Portosinusoidal vascular disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Early-onset familial noncirrhotic portal hypertension | |
| fr | Hypertension portale non cirrhotique familiale à début précoce | |
| de | Nicht-zirrhotische portale Hypertension mit frühem Beginn, familiäre Form | |
| es | Hipertensión portal no cirrótica familiar de inicio precoz | |
| it | Ipertensione portale non cirrotica familiare ad esordio precoce | |
| nl | Familiale niet-cirrotische portale hypertensie met vroege aanvang | |
| pt | Hipertensão portal não-cirrótica familiar de início precoce | |
| pl | Rodzinne niemiażdżycowe nadciścienie wrotne o wczesnym początku | |
| cs | Familiární necirhotická portální hypertenze s časným nástupem | |
| uk | Рання сімейна нециротична портальна гіпертензія | |
| zh | 家族性早发性非肝硬化门脉高压症 | |
| tr | Erken başlangıçlı ailesel sirotik olmayan portal hipertansiyon |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 617068 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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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/494348
- This record as JSON: /data/d/494348.json