ORPHA:101937
Rare pancreatic 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 pancreatic disease | |
| fr | Maladie pancréatique rare | |
| de | Pankreaskrankheit, seltene | |
| es | Enfermedad rara del páncreas | |
| it | Malattia pancreatica rara | |
| nl | Zeldzame pancreatische ziekte | |
| pt | Doença pancreática rara | |
| pl | Rzadkie choroby trzustki | |
| cs | Vzácné onemocnění pankreatu | |
| uk | Рідкісне захворювання підшлункової залози | |
| zh | 罕见胰腺疾病 | |
| tr | Nadir pankreas hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15112 | E | validated | |
| UMLS | C5681789 | E | validated | |
| GARD | 19787 | 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 (16):
- ORPHA:695131Acinar cystic transformation of the pancreas
- ORPHA:103919Autoimmune pancreatitis
- ORPHA:676Autosomal dominant hereditary chronic pancreatitis
- ORPHA:700124Autosomal recessive hereditary chronic pancreatitis
- ORPHA:313906Congenital pancreatic cyst
- ORPHA:586Cystic fibrosis
- ORPHA:309028Disorder of lipid absorption and transport
- ORPHA:300552Follicular cholangitis and pancreatitis
- ORPHA:700133Idiopathic chronic pancreatitis
- ORPHA:456312Infantile multisystem neurologic-endocrine-pancreatic disease
- ORPHA:697132Lymphoepithelial cyst of the pancreas
- ORPHA:199337Pancreatic insufficiency-anemia-hyperostosis syndrome
- ORPHA:730289Paraduodenal pancreatitis
- ORPHA:180824Rare tumor of pancreas
- ORPHA:811Shwachman-Diamond syndrome
- ORPHA:103918Tropical pancreatitis
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/101937
- This record as JSON: /data/d/101937.json