loading...| Preferred Name | Insulinoma | |
| Synonyms |
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| Definitions |
A form of functioning pancreatic neuroendocrine tumor characterized most commonly by a solitary, small pancreatic lesion that causes hyperinsulinemic hypoglycemia. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_97279 |
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| definition |
A form of functioning pancreatic neuroendocrine tumor characterized most commonly by a solitary, small pancreatic lesion that causes hyperinsulinemic hypoglycemia. |
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| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=97279 |
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| has_age_of_onset |
All ages |
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| has_inheritance |
Not applicable |
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| hasDbXref |
ICD-10:C25.4 ICD-10:D37.7 MeSH:D007340 UMLS:C0021670 ICD-11:2C10.1 MedDRA:10022498 ICD-10:D13.7 |
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| label |
Insulinoma |
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| notation |
ORPHA:97279 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_97279 |
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| prefLabel |
Insulinoma |
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| present_in |
Worldwide AND has_annual_incidence_average_value : 0.25 AND has_annual_incidence_range : 1-9 / 1 000 000 Europe AND has_point_prevalence_range : Unknown Ireland AND has_annual_incidence_average_value : 0.12 AND has_annual_incidence_range : 1-9 / 1 000 000 Japan AND has_point_prevalence_average_value : 0.56 AND has_point_prevalence_range : 1-9 / 1 000 000 |
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| treeView | ||
| subClassOf |