Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C2750063
Disease: Leber Congenital Amaurosis 14
Leber Congenital Amaurosis 14 		0.900 Biomarker MGD Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations. 21224384

2011
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C2750063
Disease: Leber Congenital Amaurosis 14
Leber Congenital Amaurosis 14 		0.900 Biomarker MGD Rpe65-/- and Lrat-/- mice: comparable models of leber congenital amaurosis. 18296659

2008
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C2750064
Disease: Retinal Dystrophy, Early-Onset Severe, Lrat-Related
Retinal Dystrophy, Early-Onset Severe, Lrat-Related 		0.600 Biomarker MGD Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations. 21224384

2011
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C2750065
Disease: RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED
RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED 		0.600 Biomarker MGD Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations. 21224384

2011
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C2750064
Disease: Retinal Dystrophy, Early-Onset Severe, Lrat-Related
Retinal Dystrophy, Early-Onset Severe, Lrat-Related 		0.600 Biomarker MGD Rpe65-/- and Lrat-/- mice: comparable models of leber congenital amaurosis. 18296659

2008
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C2750065
Disease: RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED
RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED 		0.600 Biomarker MGD Rpe65-/- and Lrat-/- mice: comparable models of leber congenital amaurosis. 18296659

2008
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations. 21224384

2011
Entrez Id: 9227
Gene Symbol: LRAT
LRAT
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		0.200 Biomarker MGD Rpe65-/- and Lrat-/- mice: comparable models of leber congenital amaurosis. 18296659

2008