raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:165658

Genetic gastro-esophageal 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
enGenetic gastro-esophageal disease
frMaladie gastro-oesophagienne génétique
deGastro-ösophageale Krankheit, genetisch bedingte
esEnfermedad gastroesofágica genética
itMalattia gastroesofagea di origine genetica
nlGenetische gastro-oesofageale ziekte
ptDoença genética gastro-esofágica
plGenetyczna choroba żołądkowo-jelitowa
csGeneticky podmíněná gastroezofageální onemocnění
ukГенетично обумовлене захворювання шлунку-стравоходу
zh遗传性胃食管疾病
trGenetik gastro-özofagus hastalığı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15617Evalidated
UMLSC5680437Evalidated

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