ORPHA:104007
Congenital enteropathy involving intestinal mucosa development
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital enteropathy involving intestinal mucosa development | |
| fr | Entéropathie congénitale liée au développement de la muqueuse intestinale | |
| de | Enteropathie mit Entwicklungsdefekt der intestinalen Mukosa, kongenitale | |
| es | Enteropatía congénita asociada al desarrollo de la mucosa intestinal | |
| it | Enteropatia congenita che interessa lo sviluppo delle mucose intestinali | |
| nl | Congenitale enteropathie met intestinale slijmvliesontwikkeling | |
| pt | Enteropatia congénita envolvendo o desenvolvimento da mucosa intestinal | |
| pl | Wrodzona enteropatia obejmująca rozwój błony śluzowej jelita | |
| cs | Vrozené enteropatie postihující vývoj střevní mukózy | |
| uk | Вроджена ентеропатія, повязана з розвитком слизової оболонки кишечника | |
| zh | 累及肠粘膜发育的先天性肠病 | |
| tr | Bağırsak mukozası gelişimini içeren doğumsal enteropati |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15182 | E | validated | |
| UMLS | C5681743 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (3):
- ORPHA:165655Genetic intestinal disease
rare genetic diseases - ORPHA:506216Rare disorder potentially indicated for bowel transplant
rare transplant-related disorders - ORPHA:117569Rare intestinal disease
rare gastroenterological diseases
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/104007
- This record as JSON: /data/d/104007.json