Human Phenotype Ontology 
Grandparent Node:
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Abdominal wall defect (HP:0010866)help
Grandparent Node:
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Hernia (HP:0100790)help
Parent Node:
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Hernia of the abdominal wall (HP:0004299)help
..Starting node
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Incisional hernia (HP:0004872)help
Term ID: 4872
Name: Incisional hernia
Synonym: Recurrent abdominal hernia
Definition: An abdominal hernia that occurs at a site of weakness in the abdominal wall resulting from an incompletely-healed surgical wound.
Comments:
Reference: HP:0004872
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFemoral hernia (HP:0100541) help
..expandInguinal hernia (HP:0000023) help
..expandOmphalocele (HP:0001539) help
..expandUmbilical hernia (HP:0001537) help
..expandVentral hernia (HP:0002933) 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:0004872HP:0004872Incisional hernia0COL1A1 CL E G H12772197ORPHA:287Classical Ehlers-Danlos syndromeHP:0040283 - Occasional373
HP:0004872HP:0004872Incisional hernia0COL5A1 CL E G H12892209ORPHA:287Classical Ehlers-Danlos syndromeHP:0040283 - Occasional660
HP:0004872HP:0004872Incisional hernia0COL5A2 CL E G H12902210ORPHA:287Classical Ehlers-Danlos syndromeHP:0040283 - Occasional325
HP:0004872HP:0004872Incisional hernia0FBN1 CL E G H22003603OMIM:154700Marfan syndrome.1361


Genes (4) :COL1A1 COL5A1 COL5A2 FBN1

Diseases (2) :ORPHA:287 OMIM:154700
 

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