ORPHA:717851

Rare non-syndromic inflammatory bowel disease

Type: Clinical group
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

9 of 12 languages

Lang	Name	Synonyms
en	Rare non-syndromic inflammatory bowel disease
fr	Maladie inflammatoire intestinale non syndromique rare
de	Seltene nicht-syndromale entzündliche Darmerkrankung
es	Enfermedad inflamatoria intestinal no sindrómica rara
it	Malattia infiammatoria rara non sindromica dell'intestino
nl	Zeldzame niet-syndromale inflammatoire darmziekte
pt	Non-syndromic inflammatory bowel disease
pl	Rare non-syndromic inflammatory bowel disease
cs	Rare non-syndromic inflammatory bowel disease

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:97935Rare gastroenterologic disease

Parents in the classifications (1):

ORPHA:104012Rare monogenic inflammatory bowel disease
rare gastroenterological diseases; rare genetic diseases; rare transplant-related disorders

Children (10):

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/717851
This record as JSON: /data/d/717851.json