| 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 |
| Similar Terms | |
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3 genes/proteins associated with the disease Hypotrichosis simplex from the curated CTD Gene-Disease Associations dataset.
