hypotrichosis Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
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)
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Genes

15 genes co-occuring with the biological term hypotrichosis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
APCDD1	adenomatosis polyposis coli down-regulated 1
CDH3	cadherin 3, type 1, P-cadherin (placental)
CDSN	corneodesmosin
DSC3	desmocollin 3
DSG4	desmoglein 4
EPS8L3	EPS8-like 3
FLG	filaggrin
HR	hair growth associated
LIPC	lipase, hepatic
LIPH	lipase, member H
LPAR6	lysophosphatidic acid receptor 6
POC1A	POC1 centriolar protein A
RPL21	ribosomal protein L21
SNRPE	small nuclear ribonucleoprotein polypeptide E
ST14	suppression of tumorigenicity 14 (colon carcinoma)