raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:275853

Syndrome with pulmonary hypertension as a major feature

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
LangNameSynonyms
enSyndrome with pulmonary hypertension as a major feature
frSyndrome avec une hypertension pulmonaire comme manifestation majeure
deSyndrom mit pulmonaler Hypertonie als HauptmerkmalSyndrom mit pulmonaler Hypertension als Hauptmerkmal
esSíndrome con hipertensión pulmonar como característica principal
itSindrome con ipertensione polmonare come segno cardinale
nlSyndroom met pulmonale hypertensie als hoofdkenmerk
ptSíndrome com hipertensão pulmonar como característica principal
plZespół z nadciśnieniem płucnym jako głównym objawem
csSyndrom s plicní hypertenzí jako hlavním příznakem
ukСиндром легеневої гіпертензії, як основний синдром
zh以肺动脉高压为主要特征的综合征
trEsas klinik özelliği pulmoner hipertansiyon olan sendrom
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO17159Evalidated
UMLSC5680755Evalidated

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):

Children (3):

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