Human Phenotype Ontology 
Grandparent Node:
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Neuroendocrine neoplasm (HP:0100634)help
Parent Node:
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Abnormality of the pancreatic islet cells (HP:0006476)help
Parent Node:
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Neoplasm of the pancreas (HP:0002894)help
Parent Node:
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Pancreatic endocrine tumor (HP:0030405)help
..Starting node
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Pancreatic islet cell adenoma (HP:0008261)help
Term ID: 8261
Name: Pancreatic islet cell adenoma
Synonym:
Definition: The presence of an adenoma of the pancreas with origin in a pancreatic B cell.
Comments:
Reference: HP:0008261
Genes and Diseases:
 
       Child Nodes:
........expandMultiple pancreatic beta-cell adenomas (HP:0008194) help
........expandInsulinoma (HP:0012197) help

 Sister Nodes: 
..expandGlucagonoma (HP:0030404) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008261HP:0008261Pancreatic islet cell adenoma0MEN1 CL E G H4221131100Multiple endocrine neoplasia, type 1131100C0025267OMIM17487010613733
HP:0008261HP:0008261Pancreatic islet cell adenoma1MEN1 CL E G H4221131100Multiple endocrine neoplasia, type 1131100C0025267OMIM17487010613733
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (6) :CDKN1A CDKN1B CDKN2B CDKN2C MAFA MEN1

Diseases (4) :131100 652 276152 147630
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.