ORPHA:165711
Rare abdominal surgical disease
- Type
- Category
- Group
- Group of disorders
- Status
- active
- Flag
- Head of classification
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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare abdominal surgical disease | |
| fr | Maladie rare en chirurgie abdominale | |
| de | Seltene Krankheiten der Abdominalchirurgie | |
| es | Enfermedad abdominal quirúrgica rara | |
| it | Malattia chirurgica addominale rara | |
| nl | Zeldzame abdominale chirurgische ziekte | |
| pt | Doença cirúrgica abdominal rara | |
| pl | Rzadka choroba operacyjna jamy brzusznej | |
| cs | Vzácné stavy v abdominální chirurgii | |
| uk | Рідкісне хірургічне захворювання органів черевної порожнини | |
| zh | 罕见腹部外科疾病 | |
| tr | Nadir görülen abdominal cerrahi hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15621 | E | validated | |
| UMLS | C5680441 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Not placed in any Orphanet classification in this release.
Children (19):
- ORPHA:93292Adenoma of pancreas
- ORPHA:228113Anal fistula
- ORPHA:293208Celiac artery compression syndrome
- ORPHA:1160Chylous ascites
- ORPHA:98043Diaphragmatic or abdominal wall malformation
- ORPHA:98039Digestive tract malformation
- ORPHA:696175Encapsulating peritoneal sclerosis
- ORPHA:438274GCGR-related hyperglucagonemia
- ORPHA:693832Gastrointestinal tract arteriovenous malformation
- ORPHA:449400IgG4-related aortitis
- ORPHA:238593IgG4-related mesenteritis
- ORPHA:49041IgG4-related retroperitoneal fibrosis
- ORPHA:306553Myospherulosis
- ORPHA:168803Primary peritoneal tumor
- ORPHA:313800ROSAH syndrome
- ORPHA:71273Renal nutcracker syndrome
- ORPHA:645793Spontaneous intestinal perforation
- ORPHA:622099Superior mesenteric artery syndrome
- ORPHA:98041Visceral malformation of the liver, biliary tract, pancreas or spleen
4
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/165711
- This record as JSON: /data/d/165711.json