raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:309005

Disorder of lipid metabolism

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
enDisorder of lipid metabolism
frTrouble du métabolisme des lipides
deFett-Stoffwechselstörung
esTrastornos del metabolismo de los lípidos
itDifetto del metabolismo dei lipidi
nlStoornis van lipidenmetabolisme
ptAlteração do metabolismo lipídico
plZaburzenia metabolizmu lipidów
csPoruchy lipidového metabolismu
ukПорушення ліпідного обміну
zh脂代谢紊乱
trLipid metabolizması bozukluğu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO2525Evalidated
MeSHD052439Evalidated
UMLSC0154251Evalidated
MedDRA10061227Evalidated

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 (4):

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