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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Ventral hernia (HP:0002933)help
Term ID: 2933
Name: Ventral hernia
Synonym:
Definition: Ventral hernia refers to a condition in which abdominal contents protrude through a weakened portion of the abdominal wall.
Comments:
Reference: HP:0002933
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFemoral hernia (HP:0100541) help
..expandIncisional hernia (HP:0004872) help
..expandInguinal hernia (HP:0000023) help
..expandOmphalocele (HP:0001539) help
..expandUmbilical hernia (HP:0001537) 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:0002933HP:0002933Ventral hernia0AEBP1 CL E G H165303ORPHA:536532Classical-like Ehlers-Danlos syndrome type 2HP:0040282 - Frequent
HP:0002933HP:0002933Ventral hernia0AEBP1 CL E G H165303OMIM:618000Ehlers-Danlos syndrome, classic-like, 2.
HP:0002933HP:0002933Ventral hernia0NXN CL E G H6435918008OMIM:618529Robinow syndrome, autosomal recessive 2.2
HP:0002933HP:0002933Ventral hernia0POGZ CL E G H2312618801ORPHA:468678White-Sutton syndromeHP:0040284 - Very rare35
HP:0002933HP:0002933Ventral hernia0TWIST2 CL E G H11758120670OMIM:200110Ablepharon-Macrostomia syndrome.7


Genes (4) :AEBP1 NXN POGZ TWIST2

Diseases (5) :ORPHA:536532 OMIM:618000 OMIM:618529 ORPHA:468678 OMIM:200110
 

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