Human Phenotype Ontology 
Grandparent Node:
expandAbnormal coronary artery origin (HP:0011636)help
Parent Node:
expandAnomalous origin of coronary artery from the pulmonary artery (HP:0011637)help
..Starting node
..expandAnomalous origin of left coronary artery from the pulmonary artery (HP:0011638)help
Term ID: 11638
Name: Anomalous origin of left coronary artery from the pulmonary artery
Synonym: ALCAPA; Anomalous left coronary artery from the pulmonary artery; Bland-Garland-White syndrome
Definition: Left main coronary artery begins (branches off from) the pulmonary artery rather than as normal from the root of the aorta, above the left cusp of the aortic valve.
Comments:
Reference: HP:0011638
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAnomalous origin of right coronary artery from the pulmonary artery (HP:0011639) help
..expandAnomalous origin of the left anterior descending artery from the pulmonary artery (HP:0031638) 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:0011638HP:0011638Anomalous origin of left coronary artery from the pulmonary artery0NADSYN1 CL E G H5519129832OMIM:618845VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3; VCRL3


Genes (1) :NADSYN1

Diseases (1) :OMIM:618845
 

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