|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Woodhouse Sakati syndrome from the curated CTD Gene-Disease Associations dataset.
|DCAF17||DDB1 and CUL4 associated factor 17||2.88009|