ORPHA:425003

Inherited digestive cancer-predisposing syndrome

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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Inherited digestive cancer-predisposing syndrome
fr	Syndrome héréditaire de prédisposition aux cancers de l'appareil digestif
de	Hereditäres Krebsprädispositionssyndrom des Verdauungssystems
es	Síndrome de predisposición al cáncer digestivo hereditario
it	Sindrome ereditaria da predisposizione ai tumori dell'apparato digerente
nl	Erfelijk digestieve kankerpredispositie-syndroom
pt	Síndrome predisponente do cancro digestivo hereditário
pl	Dziedziczny zespół predysponujący do wrodzonego raka przewodu pokarmowego
cs	Syndrom vrozené predispozice pro vznik nádoru trávicího traktu
uk	Спадковий синдром схильності до раку органів травлення
zh	遗传性消化道癌症易感综合征
tr	Kalıtsal sindirim kanserine yatkınlık sendromu

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	18538	E		validated
UMLS	C5681210	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97935Rare gastroenterologic disease

Parents in the classifications (2):

ORPHA:140162Inherited cancer-predisposing syndrome
rare genetic diseases; rare neoplastic diseases
ORPHA:97935Rare gastroenterologic disease
rare gastroenterological diseases

Children (6):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/425003
This record as JSON: /data/d/425003.json