ORPHA:104012
Rare monogenic inflammatory bowel disease
Synonyms: Rare monogenic IBD
- 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 | Rare monogenic inflammatory bowel disease | Rare monogenic IBD |
| fr | Maladie inflammatoire monogénique rare de l'intestin | Maladie inflammatoire intestinale monogénique rare · MII monogénique rare |
| de | Seltene monogene entzündliche Darmerkrankung | Seltene monogene IBD |
| es | Enfermedad inflamatoria intestinal monogénica rara | EII monogénica rara |
| it | Malattia infiammatoria intestinale monogenica rara | IBD monogenica rara |
| nl | Zeldzame monogene inflammatoire darmziekte | Zeldzame monogene IBD |
| pt | Doença inflamatória do intestino | |
| pl | Rzadka choroba zapalna jelit | = en |
| cs | Vzácná zánětlivá choroba střev | = en |
| uk | Рідкісні запальні захворювання кишечника | |
| zh | 罕见炎症性肠病 | |
| tr | Nadir iltihaplı bağırsak hastalığı |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15187 | E | validated | |
| UMLS | C5681741 | E | validated | |
| GARD | 19849 | 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
Codes that Orphanet moved or referred to this one:
- ORPHA:36205OBSOLETE: Collagenous colitis referred to · inactive
- ORPHA:58220OBSOLETE: Microscopic colitis referred to · inactive
- ORPHA:65279OBSOLETE: Lymphocytic colitis referred to · inactive
- ORPHA:103912OBSOLETE: Epithelio-exfoliative colitis-deafness syndrome referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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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/104012
- This record as JSON: /data/d/104012.json