Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536168
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Genes

1 genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GJB2 gap junction protein, beta 2, 26kDa 2.88009