Human Phenotype Ontology 
Grandparent Node:
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Abnormal circulating lipid concentration (HP:0003119)help
Parent Node:
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Hyperlipidemia (HP:0003077)help
..Starting node
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Transient hyperlipidemia (HP:0008279)help
Term ID: 8279
Name: Transient hyperlipidemia
Synonym:
Definition:
Comments:
Reference: HP:0008279
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHypertriglyceridemia (HP:0002155) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0008279HP:0008279Transient hyperlipidemia0CPT1A CL E G H1374156ORPHA15032328600528
HP:0008279HP:0008279Transient hyperlipidemia0CPT1A CL E G H1374156ORPHA14522328600528
HP:0008279HP:0008279Transient hyperlipidemia0CPT1A CL E G H1374255120Carnitine palmitoyltransferase I deficiency255120C0342789OMIM15032328600528
HP:0008279HP:0008279Transient hyperlipidemia0CPT1A CL E G H1374255120Carnitine palmitoyltransferase I deficiency255120C0342789OMIM14522328600528
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :CPT1A

Diseases (2) :156 255120
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.