raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:79174

Disorder of fatty acid oxidation and ketone body 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 fatty acid oxidation and ketone body metabolism
frTrouble de l'oxydation des acides gras et du métabolisme des corps cétoniques
deFettsäureoxidationsstörungen und Ketogenesedefekt
esTrastornos de la oxidación de los ácidos grasos y del metabolismo de los cuerpos cetónicos
itDifetto dell'ossidazione degli acidi grassi e del metabolismo dei corpi chetonici
nlStoornis van vetzuuroxidatie en ketonlichaammetabolisme
ptDoença da oxidação dos ácidos gordos ou da cetogénese
plZaburzenie oksydacji kwasów tłuszczowych i metabolizmu ciał ketonowych
csPorucha oxidace mastných kyselin a metabolismu ketolátek
ukПорушення окислення жирних кислот і метаболізму кетонових тіл
zh脂肪酸氧化和酮体代谢异常
trYağ asidi oksidasyonu ve keton cisimciği metabolizması bozukluğu
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10E71.3Especificvalidated
MONDO0019223Evalidated
MONDO19223Evalidated
UMLSC5681281Evalidated

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 (5):

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