DOID:4535 - hypotrichosis
Disease Ontology Definition: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.
Xenbase Genes : cdh3, tgif1, rpl21, apcdd1, liph, snrpe, lpar6
|MONDO:0003037 - hypotrichosis|
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hair disease (is_a)