|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A skin disease characterized by skin that is loose, hanging, wrinkled and lacking in elasticity; it can also affect connective tissue in other parts of the body, including the heart, blood vessels, joints, intestines and lungs. (Human Disease Ontology, DOID_3144)|
|Downloads & Tools|
2 genes/proteins associated with the disease Cutis Laxa from the curated CTD Gene-Disease Associations dataset.