Abnormal Internal Carotid Artery Morphology Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	any structural anomaly of the terminal branch of the left or right common carotid artery which supplies oxygenated blood to the brain and eyes (Mammalian Phenotype Ontology, MP_0012730)
External Link	https://www.disgenet.org/browser/0/1/0/C1860488
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Genes

7 genes associated with the disease Abnormal Internal Carotid Artery Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ABCG5	ATP-binding cassette, sub-family G (WHITE), member 5
ABCG8	ATP-binding cassette, sub-family G (WHITE), member 8
APOB	apolipoprotein B
LDLR	low density lipoprotein receptor
LDLRAP1	low density lipoprotein receptor adaptor protein 1
NDE1	nudE neurodevelopment protein 1
PCSK9	proprotein convertase subtilisin/kexin type 9