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loading...| Preferred Name | Islet_Cell_Hyperplasia | |
| Synonyms |
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|
| ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Islet_Cell_Hyperplasia |
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| ID |
C4375 |
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| NCI_Definition |
A sporadic or inherited disorder characterized by the focal or diffuse proliferation of the cells of the islets of Langerhans in the pancreas. It results in hyperinsulinemia and hypoglycemia. |
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| NCI_PT |
Nesidioblastosis |
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| NICHD_Definition |
_ |
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| prefixIRI |
Islet_Cell_Hyperplasia |
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| prefLabel |
Islet_Cell_Hyperplasia |
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| Subset_Association1 |
NICHD Pediatric Terminology |
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| Subset_Association2 |
Neonatal Research Network Terminology |
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| SYN | ||
| subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Endocrine_System_Disorder |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/SNOMEDCT/42681006 | SNOMEDCT | LOOM | |
| http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1145 | IFAR | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/MTHU023473 | OMIM | LOOM |