Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3265
Gene Symbol: HRAS
HRAS
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		0.710 Biomarker GENOMICS_ENGLAND Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia. 24006476

2014
Entrez Id: 3265
Gene Symbol: HRAS
HRAS
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		0.710 SomaticCausalMutation ORPHANET Mosaicism for HRAS c.37G>C and KRAS c.35G>A mutations was found in two individuals with Schimmelpenning syndrome. 22683711

2012
Entrez Id: 3265
Gene Symbol: HRAS
HRAS
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		0.710 Biomarker CTD_human Mosaicism for HRAS c.37G>C and KRAS c.35G>A mutations was found in two individuals with Schimmelpenning syndrome. 22683711

2012
Entrez Id: 3265
Gene Symbol: HRAS
HRAS
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		0.710 Biomarker GENOMICS_ENGLAND Germline mutations in HRAS proto-oncogene cause Costello syndrome. 16170316

2005
Entrez Id: 3265
Gene Symbol: HRAS
HRAS
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis 		0.710 Biomarker GENOMICS_ENGLAND