raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:70470

OBSOLETE: Hyperlipoproteinemia type 5

inactive · referred to ORPHA:444490Familial chylomicronemia syndrome

Synonyms: OBSOLETE: HLP type 5 · OBSOLETE: Major hyperlipidemia

Type
Disease
Group
Disorder
Status
inactive
Flag
Obsolete entity

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

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Hyperlipoproteinemia type 5OBSOLETE: HLP type 5 · OBSOLETE: Major hyperlipidemia
frOBSOLETE : Hyperlipoprotéinémie type 5OBSOLETE : HLP type 5 · OBSOLETE : Hyperlipidémie majeure
deOBSOLET: Hyperlipoproteinämie Typ 5OBSOLET: HLP Typ 5 · OBSOLET: Major hyperlipidemia
esOBSOLETO: Hiperlipoproteinemia tipo 5OBSOLETO: HLP tipo 5 · OBSOLETO: Hiperlipidemia grave
itOBSOLETO: Iperlipoproteinemia, tipo 5OBSOLETO: HLP tipo 5 · OBSOLETO: Iperlipidemia maggiore
nlOBSOLEET: Hyperlipoproteïnemie type 5OBSOLEET: HLP type 5 · OBSOLEET: Majeure hyperlipidemie
ptOBSOLETO: Hiperlipoproteinemia tipo 5OBSOLETO: Hiperlipidemia major
plNIEAKTUALNE: Hiperlipoproteinemia typu 5NIEAKTUALNE: Major hyperlipidemia
csNEAKTUÁLNÍ: Hyperlipoproteinémie, typ 5NEAKTUÁLNÍ: Hlavní hyperlipidémie
ukЗАСТАРІЛО: Гіперліпопротеїнемія, тип 5ЗАСТАРІЛО: HLP тип 5 · ЗАСТАРІЛО: Поширена гіперліпідемія
zh弃用：高脂蛋白血症5型主要高脂血症
trEski adı: Hiperlipoproteinemi tip 5HLP tip 5 · Major hiperlipidemi
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