Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3265
Gene Symbol: HRAS
HRAS
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		0.310 GeneticVariation BEFREE PTPN11 (39.0%), SOS1 (20.3%), RAF1 (6.8%), KRAS (5.1%), and BRAF (1.7%) mutations were identified in NS; BRAF (41.2%), SHOC2 (23.5%), and MEK1 (5.9%) mutations in cardiofaciocutaneous syndrome; and HRAS and PTPN11 mutations in Costello syndrome and LEOPARD syndrome, respectively. 21784453

2011
Entrez Id: 3265
Gene Symbol: HRAS
HRAS
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome 		0.310 Biomarker CLINGEN