Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.410 GeneticVariation disease BEFREE We identify new CBD susceptibility loci and show that CBD and PSP share a genetic risk factor other than MAPT at 3p22 MOBP (myelin-associated oligodendrocyte basic protein). 26077951 2016
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.410 GeneticVariation disease GWASDB We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.410 GeneticVariation disease GWASCAT We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
0.410 Biomarker disease CTD_human We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. 21685912 2011
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
0.400 Biomarker disease CTD_human Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. 27455348 2016
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
0.400 GeneticVariation disease GWASCAT Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. 27455348 2016
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
0.310 Biomarker disease BEFREE Gene level disturbances in cellular and molecular networks impacted by alcohol and alcoholism pathology include transketolase (TKT), transferrin (TF), and myelin (e.g., MBP, MOBP, and MOG). 25655461 2015
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
0.310 Biomarker disease PSYGENET Gene level disturbances in cellular and molecular networks impacted by alcohol and alcoholism pathology include transketolase (TKT), transferrin (TF), and myelin (e.g., MBP, MOBP, and MOG). 25655461 2015
Amyotrophic Lateral Sclerosis With Dementia
0.300 Biomarker disease CTD_human Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. 27455348 2016
Amyotrophic Lateral Sclerosis, Guam Form
0.300 Biomarker disease CTD_human Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. 27455348 2016
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.100 GeneticVariation disease GWASCAT Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. 28931804 2018
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1
0.100 GeneticVariation disease GWASCAT Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. 28931804 2018
Amyotrophic Lateral Sclerosis, Sporadic
0.100 GeneticVariation disease GWASCAT Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. 28931804 2018
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
0.100 GeneticVariation disease GWASCAT Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. 28931804 2018
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.100 GeneticVariation disease GWASCAT Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033 2014
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.100 GeneticVariation disease GWASDB Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. 23535033 2014
CUI: C0004509
Disease: Azoospermia
Azoospermia
0.100 GeneticVariation disease GWASDB A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. 22197933 2012
Attention deficit hyperactivity disorder
0.100 GeneticVariation disease GWASDB Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. 18839057 2009
Attention deficit hyperactivity disorder
0.100 GeneticVariation disease GWASCAT Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. 18839057 2009
COLORBLINDNESS, PARTIAL, DEUTAN SERIES
0.010 GeneticVariation disease BEFREE We identify new CBD susceptibility loci and show that CBD and PSP share a genetic risk factor other than MAPT at 3p22 MOBP (myelin-associated oligodendrocyte basic protein). 26077951 2016
CUI: C0002893
Disease: Refractory anemias
Refractory anemias
0.010 Biomarker disease BEFREE MOBP RA+ patients have more severe white matter degeneration in bvFTD that may contribute to shorter disease duration. 24994843 2014
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 Biomarker disease BEFREE MOBP RA+ patients have more severe white matter degeneration in bvFTD that may contribute to shorter disease duration. 24994843 2014
CUI: C0949664
Disease: Tauopathies
Tauopathies
0.010 GeneticVariation group BEFREE Eighty-one patients with sporadic bvFTD were genotyped for tauopathy-associated SNPs at rs8070723 (microtubule-associated protein tau [MAPT]) and rs1768208 (myelin-associated oligodendrocyte basic protein [MOBP]). 24994843 2014
Behavioral variant of frontotemporal dementia
0.010 Biomarker disease BEFREE MOBP RA+ patients have more severe white matter degeneration in bvFTD that may contribute to shorter disease duration. 24994843 2014
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 AlteredExpression disease BEFREE Correlation and factor analyses revealed that mRNA levels for genes that did exhibit differential expression in schizophrenia (MAG, CNP, SOX10, CLDN11, and PMP2), as opposed to those that did not (MOBP and MBP), loaded on separate factors. 16213148 2006