ORPHA:717865

Rare congenital/chronic/intractable diarrhea 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 congenital/chronic/intractable diarrhea with inflammatory bowel disease
fr	Diarrhée congénitale/chronique/réfractaire rare avec maladie inflammatoire de l'intestin
de	Seltene kongenitale chronische therapieresistente Diarrhoe mit entzündlicher Darmerkrankung
es	Diarrea congénita rara crónica e intratable con enfermedad inflamatoria intestinal
it	Diarrea congenita cronica non trattabile rara con malattia infiammatoria dell'intestino
nl	Zeldzame congenitale/chronische/therapieresistente diarree met inflammatoire darmziekte
pt	Congenital-chronic-intractable diarrhea with inflammatory bowel disease
pl	Rare congenital/chronic/intractable diarrhea with inflammatory bowel disease
cs	Rare congenital/chronic/intractable diarrhea 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:717862Rare disorder with inflammatory bowel disease
rare gastroenterological diseases; rare genetic diseases; rare transplant-related disorders

Children (5):

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/717865
This record as JSON: /data/d/717865.json