Hypotrichosis simplex Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Hypotrichosis simplex (HS) or hereditary hypotrichosis simplex (HHS) is characterized by reduced pilosity over the scalp and body (with sparse, thin, and short hair) in the absence of other anomalies. (Orphanet Rare Disease Ontology, Orphanet_55654)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537160
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3 genes/proteins associated with the disease Hypotrichosis simplex from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
LPAR6 lysophosphatidic acid receptor 6 2.88009
APCDD1 adenomatosis polyposis coli down-regulated 1 2.88009
TGIF1 TGFB-induced factor homeobox 1 2.88009