|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A pigmentation disease characterized by a reticulate pattern of abnormally dark skin coloring, particularly in the body's folds and creases. (Human Disease Ontology, DOID_0060256)|
|Downloads & Tools|
1 genes/proteins associated with the disease dowling-degos disease from the curated CTD Gene-Disease Associations dataset.
|KRT5||keratin 5, type II||2.88009|