| 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 |
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 |
