| Preferred Name |
Nesidioblastosis |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C4375 |
| code |
C4375 |
| Concept_In_Subset | |
| Contributing_Source |
NICHD |
| 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. |
| FULL_SYN |
Islet Cell Adenomatosis |
| Has_NICHD_Parent | |
| label |
Nesidioblastosis |
| Legacy_Concept_Name |
Islet_Cell_Adenomatosis |
| Neoplastic_Status |
Undetermined |
| NICHD_Hierarchy_Term |
Nesidioblastosis |
| Preferred_Name |
Nesidioblastosis |
| prefixIRI |
C4375 |
| prefLabel |
Nesidioblastosis |
| Semantic_Type |
Disease or Syndrome Neoplastic Process |
| UMLS_CUI |
C0027773 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MESH/D046768 | Medical Subject Headings | LOOM |