|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Kabuki syndrome (KS) is a multiple congenital anomaly syndrome characterized by typical facial features, skeletal anomalies, mild to moderate intellectual disability and postnatal growth deficiency. (Orphanet Rare Disease Ontology, Orphanet_2322)|
|Downloads & Tools|
1 genes/proteins associated with the disease Kabuki syndrome from the curated CTD Gene-Disease Associations dataset.
|KMT2D||lysine (K)-specific methyltransferase 2D||2.88009|