ORPHA:506216
Rare disorder potentially indicated for bowel transplant
- 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 disorder potentially indicated for bowel transplant | |
| fr | Maladie rare possiblement indiquée pour la transplantation intestinale | |
| de | Seltene Erkrankung zur potentiellen Darm-Transplantation indiziert | |
| es | Trastorno raro potencialmente indicado para trasplante de intestino | |
| it | Malattia rara con indicazione al trapianto intestinale | |
| nl | Zeldzame aandoening mogelijk geïndiceerd voor darmtransplantatie | |
| pt | Doença rara com potencial indicação para transplante intestinal | |
| pl | Choroba rzadka będąca potencjalnym wskazaniem do przeszczepu jelita | |
| cs | Vzácná porucha indikovaná k transplantaci střeva | |
| uk | Рідкісне захворювання, яке може бути показанням для трансплантації кишківника | |
| zh | 可能适用于肠道移植的罕见疾病 | |
| tr | Bağırsak nakli için potansiyel olarak endike olan nadir hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681213 | 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):
- ORPHA:565779Rare disorder potentially indicated for transplant or complication after transplantation
Parents in the classifications (1):
- ORPHA:506207Rare disorder potentially indicated for transplant
rare transplant-related disorders
Children (16):
- ORPHA:96346Anorectal malformation
- ORPHA:294422Chronic intestinal failure
- ORPHA:104007Congenital enteropathy involving intestinal mucosa development
- ORPHA:104003Congenital intestinal transport defect
- ORPHA:313906Congenital pancreatic cyst
- ORPHA:468635Cryptogenic multifocal ulcerous stenosing enteritis
- ORPHA:71274Disseminated peritoneal leiomyomatosis
- ORPHA:97945Intestinal malformation
- ORPHA:104010Intestinal polyposis syndrome
- ORPHA:73014Intractable diarrhea of infancy
- ORPHA:108971Non-syndromic visceral malformation of the liver, biliary tract, pancreas or spleen
- ORPHA:168807Primary malignant peritoneal tumor
- ORPHA:104009Rare disease involving intestinal motility
- ORPHA:104012Rare monogenic inflammatory bowel disease
- ORPHA:104011Rare tumor of intestine
- ORPHA:104008Short bowel syndrome
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/506216
- This record as JSON: /data/d/506216.json