raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:699068

Fontan-associated liver disease

Synonyms: FALD

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
Adolescent, Adult, Childhood
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

9 of 12 languages
LangNameSynonyms
enFontan-associated liver diseaseFALD
frMaladie hépatique associée à l'intervention de Fontan= en
deFontan-assoziierte Lebererkrankung= en
esEnfermedad hepática asociada al síndrome de FontanEHCF · Enfermedad hepática relacionada con cirugía de Fontan · FALD
itEpatopatia associata a Fontan= en
nlFontan-geassocieerde leverziekteAandoening van lever na Fontan-operatie · FALD
ptFontan-associated liver disease
plFontan-associated liver disease= en
csFontan-associated liver disease= en
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (4):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalence1-9 / 1 000 0000 / 100 000WorldwideValue and classValidatedORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card