Hyperkeratosis lenticularis perstans Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Hyperkeratosis lenticularis perstans (HLP), also known as Flegel disease, is a keratinization abnormality characterized by small, asymptomatic erythematous papules that leave characteristic punctate bleeding when they become detached. The lesions generally occur symmetrically along the top of the foot and on the legs, appearing more rarely on the arms, forearms, palms, and soles, and even on the oral mucosa. (Human Phenotype Ontology, HP_0007570)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C538377
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Hyperkeratosis lenticularis perstans from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HLP hyperkeratosis lenticularis perstans 2.88009