ORPHA:365563
Primary short bowel syndrome
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Primary short bowel syndrome | |
| fr | Syndrome du grêle court primaire | Syndrome de l'intestin court primaire · SGC primaire |
| de | Kurzdarm-Syndrom, primäres | |
| es | Síndrome primario del intestino corto | |
| it | Sindrome dell'intestino corto primitiva | |
| nl | Primair kortedarmsyndroom | |
| pt | Síndrome primária do intestino curto | |
| pl | Pierwotny zespół krótkiego jelita | |
| cs | Primární syndrom krátkého střeva | |
| uk | Первинний синдром короткої кишки | |
| zh | 原发性短肠综合征 | |
| tr | Primer kısa bağırsak sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18241 | E | validated | |
| UMLS | C5680971 | 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 (2):
- ORPHA:165655Genetic intestinal disease
rare genetic diseases - ORPHA:104008Short bowel syndrome
rare gastroenterological diseases; rare transplant-related disorders
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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.
6
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/365563
- This record as JSON: /data/d/365563.json