ORPHA:165661
Genetic 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 | Genetic pancreatic disease | |
| fr | Maladie pancréatique génétique | |
| de | Pankreaskrankheit, genetisch bedingte | |
| es | Enfermedad genética pancreática | |
| it | Malattia pancreatica di origine genetica | |
| nl | Genetische aandoening van pancreas | Genetische ziekte van alvleesklier |
| pt | Doença genética pancreática | |
| pl | Genetyczna choroba trzustki | |
| cs | Geneticky podmíněná onemocnění pankreatu | |
| uk | Генетично обумовлене захворювання підшлункової залози | |
| zh | 遗传性胰腺病 | |
| tr | Genetik pankreas hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15618 | E | validated | |
| UMLS | C5680436 | 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:165652Rare genetic gastroenterological disease
rare genetic diseases
Children (8):
- ORPHA:676Autosomal dominant hereditary chronic pancreatitis
- ORPHA:700124Autosomal recessive hereditary chronic pancreatitis
- ORPHA:586Cystic fibrosis
- ORPHA:309028Disorder of lipid absorption and transport
- ORPHA:1333Familial pancreatic carcinoma
- ORPHA:456312Infantile multisystem neurologic-endocrine-pancreatic disease
- ORPHA:199337Pancreatic insufficiency-anemia-hyperostosis syndrome
- ORPHA:811Shwachman-Diamond 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/165661
- This record as JSON: /data/d/165661.json