Human Phenotype Ontology 
Grandparent Node:
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Ventricular septal defect (HP:0001629)help
Parent Node:
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Muscular ventricular septal defect (HP:0011623)help
..Starting node
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Apical muscular ventricular septal defect (HP:0011624)help
Term ID: 11624
Name: Apical muscular ventricular septal defect
Synonym:
Definition: A muscular ventricular septal defect located at the apex of the heart.
Comments:
Reference: HP:0011624
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMultiple muscular ventricular septal defects (HP:0011625) 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:0011624HP:0011624Apical muscular ventricular septal defect0 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.