raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enEarly-onset familial noncirrhotic portal hypertension
frHypertension portale non cirrhotique familiale à début précoce
deNicht-zirrhotische portale Hypertension mit frühem Beginn, familiäre Form
esHipertensión portal no cirrótica familiar de inicio precoz
itIpertensione portale non cirrotica familiare ad esordio precoce
nlFamiliale niet-cirrotische portale hypertensie met vroege aanvang
ptHipertensão portal não-cirrótica familiar de início precoce
plRodzinne niemiażdżycowe nadciścienie wrotne o wczesnym początku
csFamiliární necirhotická portální hypertenze s časným nástupem
ukРання сімейна нециротична портальна гіпертензія
zh家族性早发性非肝硬化门脉高压症
trErken başlangıçlı ailesel sirotik olmayan portal hipertansiyon

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM617068Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card