Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the pancreas (HP:0001732)help
Parent Node:
expandAbnormal pancreas morphology (HP:0012090)help
..Starting node
..expandPancreas divisum (HP:0030994)help
Term ID: 30994
Name: Pancreas divisum
Synonym:
Definition: A congenital anomaly of the pancreas that results from failed fusion of the dorsal and ventral ducts during embyological development. Three variants have been described: type 1 or classical divisum in which there is total failure of fusion; type 2 in which dorsal drainage is dominant in the absence of the duct of Wirsung; and type 3 or incomplete divisum where a small communicating branch is present.
Comments:
Reference: HP:0030994
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal pancreas size (HP:0012094) help
..expandAbnormal pancreatic duct morphology (HP:0030992) help
..expandAnnular pancreas (HP:0001734) help
..expandEctopic pancreatic tissue (HP:0006278) help
..expandHyperechogenic pancreas (HP:0006276) help
..expandPancreatic abscess (HP:0025079) help
..expandPancreatic calcification (HP:0005213) help
..expandPancreatic cysts (HP:0001737) help
..expandPancreatic dysplasia (HP:0005232) help
..expandPancreatic fibrosis (HP:0100732) help
..expandPancreatic fistula (HP:0100844) help
..expandPancreatic lymphangiectasis (HP:0006273) help
..expandPancreatic pseudocyst (HP:0005206) 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:0030994HP:0030994Pancreas divisum0 CL E G H


Genes (0) :

Diseases (0) :
 

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