raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:181425

OBSOLETE: Rare major hypertriglyceridemia

inactive · referred to ORPHA:181422Rare hyperlipidemia

Type
Category
Group
Group of disorders
Status
inactive
Flag
Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare hyperlipidemia

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Rare major hypertriglyceridemia
frOBSOLETE : Hypertriglycéridémie majeure rare
deOBSOLET: Hypertriglyceridämie, Major-Form
esOBSOLETO: Hipertrigliceridemia grave rara
itOBSOLETO: Ipertrigliceridemia major
nlOBSOLEET: Zeldzame majeure hypertriglyceridemie
ptOBSOLETO: Hipertrigliceridemia major
plNIEAKTUALNE: Rzadka, ciężka hipertriglicerydemia
csNEAKTUÁLNÍ: Hypertriglyceridemia major
ukЗАСТАРІЛО: Рідкісна значна гіпертригліцеридемія
zh弃用:罕见主要高甘油三酯血症
trEski adı: Nadir majör hipertrigliseridemi
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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