ORPHA:117569
Rare intestinal 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare intestinal disease | |
| fr | Maladie intestinale rare | |
| de | Intestinale Krankheit, seltene | |
| es | Enfermedad intestinal rara | |
| it | Malattia intestinale rara | |
| nl | Zeldzame darmziekte | |
| pt | Intestinal, doença rara | |
| pl | Rzadka choroba jelit | |
| cs | Vzácná střevní onemocnění | |
| uk | Рідкісні кишкові захворювання | |
| zh | 罕见肠道疾病 | |
| tr | Nadir bağırsak hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15245 | E | validated | |
| UMLS | C5681751 | E | validated | |
| GARD | 19873 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:97935Rare gastroenterologic disease
rare gastroenterological diseases
Children (36):
- ORPHA:228113Anal fistula
- ORPHA:1116Aplasia cutis congenita-intestinal lymphangiectasia syndrome
- ORPHA:160148Cap polyposis
- ORPHA:435988Chronic atrial and intestinal dysrhythmia syndrome
- ORPHA:294422Chronic intestinal failure
- ORPHA:104007Congenital enteropathy involving intestinal mucosa development
- ORPHA:104006Congenital intestinal disease due to an enzymatic defect
- ORPHA:104003Congenital intestinal transport defect
- ORPHA:468635Cryptogenic multifocal ulcerous stenosing enteritis
- ORPHA:477787Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder
- ORPHA:693832Gastrointestinal tract arteriovenous malformation
- ORPHA:238621Ileal pouch anal anastomosis related faecal incontinence
- ORPHA:104005Intestinal disease due to fat malabsorption
- ORPHA:104004Intestinal disease due to vitamin absorption anomaly
- ORPHA:36204Intestinal lymphangiectasia
- ORPHA:73014Intractable diarrhea of infancy
- ORPHA:583861Isolated mesenteric vein thrombosis
- ORPHA:556Malakoplakia
- ORPHA:104013Metabolic disease with intestinal involvement
- ORPHA:263665NK-cell enteropathy
- ORPHA:391673Necrotizing enterocolitis
- ORPHA:217067Pouchitis
- ORPHA:397606PrP systemic amyloidosis
- ORPHA:565641Primary desmosis coli
- ORPHA:70475Radiation proctitis
- ORPHA:104009Rare disease involving intestinal motility
- ORPHA:104012Rare monogenic inflammatory bowel disease
- ORPHA:104011Rare tumor of intestine
- ORPHA:398063Refractory celiac disease
- ORPHA:3130Satoyoshi syndrome
- ORPHA:94075Severe immune-mediated enteropathy
- ORPHA:104008Short bowel syndrome
- ORPHA:209964Solitary rectal ulcer syndrome
- ORPHA:645793Spontaneous intestinal perforation
- ORPHA:622099Superior mesenteric artery syndrome
- ORPHA:3452Whipple disease
Codes that Orphanet moved or referred to this one:
- ORPHA:103920OBSOLETE: Undetermined colitis referred to · inactive
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/117569
- This record as JSON: /data/d/117569.json