Chromosome Xp11.3 Deletion 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:C564481
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Genes

2 genes/proteins associated with the disease Chromosome Xp11.3 Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
RP2 retinitis pigmentosa 2 (X-linked recessive) 2.88009
DELXP11.3 Chromosome Xp11.3 deletion syndrome 2.88009