Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the pancreatic islet cells (HP:0006476)help
Grandparent Node:
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Neoplasm of the pancreas (HP:0002894)help
Grandparent Node:
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Pancreatic endocrine tumor (HP:0030405)help
Parent Node:
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Pancreatic islet cell adenoma (HP:0008261)help
..Starting node
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Multiple pancreatic beta-cell adenomas (HP:0008194)help
Term ID: 8194
Name: Multiple pancreatic beta-cell adenomas
Synonym:
Definition: The presence of multiple pancreatic islet cell adenomas.
Comments:
Reference: HP:0008194
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandInsulinoma (HP:0012197) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008194HP:0008194Multiple pancreatic beta-cell adenomas0KCNJ11 CL E G H37676257ORPHA:79644Autosomal recessive hyperinsulinism due to Kir6.2 deficiency127
HP:0008194HP:0008194Multiple pancreatic beta-cell adenomas0MAFA CL E G H38969223145OMIM:147630Insulinomatosis and diabetes mellitus.


Genes (2) :KCNJ11 MAFA

Diseases (2) :ORPHA:79644 OMIM:147630
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.