Hypotrichosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles. (Human Disease Ontology, DOID_4535)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D007039
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3 genes/proteins associated with the disease Hypotrichosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
LPAR6 lysophosphatidic acid receptor 6 2.88009
DSG4 desmoglein 4 2.88009
LIPH lipase, member H 2.88009