Hypotrichosis simplex Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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://www.omim.org/entry/605389
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Genes

1 genes associated with the Hypotrichosis simplex phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
APCDD1 adenomatosis polyposis coli down-regulated 1