Cutis Laxa Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link
Similar Terms
Downloads & Tools


2 genes/proteins associated with the disease Cutis Laxa from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ELN elastin 2.88009
PYCR1 pyrroline-5-carboxylate reductase 1 2.88009