Woodhouse Sakati syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia. (Orphanet Rare Disease Ontology, Orphanet_3464)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536742
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1 genes/proteins associated with the disease Woodhouse Sakati syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DCAF17 DDB1 and CUL4 associated factor 17 2.88009