raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:156601

Rare genetic hepatic disease

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
enRare genetic hepatic disease
frMaladie hépatique génétique rare
deLeberkrankheit, genetische, seltene
esEnfermedades hepáticas genéticas raras
itMalattia epatica genetica
nlZeldzame genetische leverziekteZeldzame genetische aandoening van lever
ptDoença hepática genética
plRzadka genetyczna choroba wątroby
csVzácná geneticky podmíněná onemocnění jater
ukРідкісне генетично обумовлене захворювання печінки
zh罕见遗传性肝病
trNadir genetik karaciğer hastalığı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15507Evalidated
UMLSC5680645Evalidated

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 (7):

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