SEMA4A, semaphorin 4A, 64218

N. diseases: 141; N. variants: 5
Disease: RETINITIS PIGMENTOSA 35 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1853214
Disease: RETINITIS PIGMENTOSA 35
RETINITIS PIGMENTOSA 35 		0.700 GeneticVariation disease UNIPROT SEMA4A mutations lead to susceptibility to light irradiation, oxidative stress, and ER stress in retinal pigment epithelial cells. 22956603 2012
CUI: C1853214
Disease: RETINITIS PIGMENTOSA 35
RETINITIS PIGMENTOSA 35 		0.700 GeneticVariation disease UNIPROT Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases. 16199541 2006
CUI: C1853214
Disease: RETINITIS PIGMENTOSA 35
RETINITIS PIGMENTOSA 35 		0.700 Biomarker disease GENOMICS_ENGLAND Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases. 16199541 2006
CUI: C1853214
Disease: RETINITIS PIGMENTOSA 35
RETINITIS PIGMENTOSA 35 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1853214
Disease: RETINITIS PIGMENTOSA 35
RETINITIS PIGMENTOSA 35 		0.700 Biomarker disease CTD_human
CUI: C1853214
Disease: RETINITIS PIGMENTOSA 35
RETINITIS PIGMENTOSA 35 		0.700 CausalMutation disease CLINVAR