ORPHA:700136
Early-onset idiopathic chronic pancreatitis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Early-onset idiopathic chronic pancreatitis | |
| fr | Pancréatite chronique idiopathique précoce | |
| de | Pankreatitis, chronische idiopathische, früh beginnende | |
| es | Pancreatitis crónica idiopática de inicio precoz | |
| it | Pancreatite cronica idiopatica ad esordio precoce | |
| nl | Vroeg optredende idiopathische chronische pancreatitis | Vroeg optredende idiopathische chronische alvleesklierontsteking |
| pt | Early-onset idiopathic chronic pancreatitis | |
| pl | Early-onset idiopathic chronic pancreatitis | |
| cs | Early-onset idiopathic chronic pancreatitis |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:700133Idiopathic chronic pancreatitis
rare gastroenterological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 6 / 100 000 | Worldwide | Value and class | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/700136
- This record as JSON: /data/d/700136.json