ORPHA:717862

Rare disorder with inflammatory bowel 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.

Names in Orphadata languages

9 of 12 languages

Lang	Name	Synonyms
en	Rare disorder with inflammatory bowel disease
fr	Maladie rare avec maladie inflammatoire de l'intestin
de	Seltene Störung mit entzündlicher Darmerkrankung
es	Trastorno raro con enfermedad inflamatoria intestinal
it	Malattia rara con malattia infiammatoria dell'intestino
nl	Zeldzame ziekte met inflammatoire darmziekte
pt	Rare disorder with inflammatory bowel disease
pl	Rare disorder with inflammatory bowel disease
cs	Rare disorder with 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 (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/717862
This record as JSON: /data/d/717862.json