Kabuki syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C537705
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1 genes/proteins associated with the disease Kabuki syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
KMT2D lysine (K)-specific methyltransferase 2D 2.88009