dowling-degos disease Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C562924
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Genes

1 genes/proteins associated with the disease dowling-degos disease from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
KRT5 keratin 5, type II 2.88009