Human Phenotype Ontology 
Grandparent Node:
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Conotruncal defect (HP:0001710)help
Parent Node:
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Absence of the pulmonary valve (HP:0005134)help
Parent Node:
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Tetralogy of Fallot (HP:0001636)help
..Starting node
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Tetralogy of Fallot with absent pulmonary valve (HP:0011659)help
Term ID: 11659
Name: Tetralogy of Fallot with absent pulmonary valve
Synonym: Tetralogy of Fallot with absent pulmonary valve syndrome
Definition: Features of tetralogy of Fallot with either rudimentary ridges or the complete absence of pulmonic valve tissue.
Comments:
Reference: HP:0011659
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandTetralogy of Fallot with absent subarterial conus (HP:0011676) help
..expandTetralogy of Fallot with atrioventricular canal defect (HP:0011677) help
..expandTetralogy of Fallot with pulmonary atresia (HP:0012516) help
..expandTetralogy of Fallot with pulmonary stenosis (HP:0011679) 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:0011659HP:0011659Tetralogy of Fallot with absent pulmonary valve0 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.