|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the arterial tortuosity syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|SLC2A10||solute carrier family 2 (facilitated glucose transporter), member 10|