hypotrichosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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://compbio.charite.de/hpoweb/showterm?id=HP:0001006
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21 genes associated with the hypotrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANTXR1 anthrax toxin receptor 1
APCDD1 adenomatosis polyposis coli down-regulated 1
CDH3 cadherin 3, type 1, P-cadherin (placental)
CDSN corneodesmosin
CLDN1 claudin 1
DSC3 desmocollin 3
DSG1 desmoglein 1
EDA ectodysplasin A
EDAR ectodysplasin A receptor
HOXC13 homeobox C13
HR hair growth associated
KRT74 keratin 74, type II
KRT81 keratin 81, type II
KRT83 keratin 83, type II
KRT86 keratin 86, type II
LPAR6 lysophosphatidic acid receptor 6
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
SOX18 SRY (sex determining region Y)-box 18
TGM1 transglutaminase 1
WNT10A wingless-type MMTV integration site family, member 10A