Silver-Russell Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_14681)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D056730
Similar Terms
Downloads & Tools

Genes

6 genes/proteins associated with the disease Silver-Russell Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
IGF2 insulin-like growth factor 2 2.88009
H19 H19, imprinted maternally expressed transcript (non-protein coding) 2.88009
FOXP2 forkhead box P2 2.88009
GH2 growth hormone 2 2.88009
CSH1 chorionic somatomammotropin hormone 1 (placental lactogen) 2.88009
RSS Russell Silver syndrome 2.88009