arterial tortuosity syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A connective tissue disease that is characterized by elongation and generalized tortuosity of the major arteries including the aorta. (Human Disease Ontology, DOID_0050645)
External Link http://www.omim.org/entry/208050
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Genes

1 genes associated with the arterial tortuosity syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10