Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C3151411
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 6
MENTAL RETARDATION, AUTOSOMAL DOMINANT 6 		0.700 CausalMutation CLINVAR Utility of Whole Exome Sequencing for Genetic Diagnosis of Previously Undiagnosed Pediatric Neurology Patients. 27572814

2016
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C4015316
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27 		0.700 CausalMutation CLINVAR Utility of Whole Exome Sequencing for Genetic Diagnosis of Previously Undiagnosed Pediatric Neurology Patients. 27572814

2016
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764

2015
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C3151411
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 6
MENTAL RETARDATION, AUTOSOMAL DOMINANT 6 		0.700 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C4015316
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27 		0.700 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.650 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.470 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.430 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0037769
Disease: West Syndrome
West Syndrome 		0.420 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		0.410 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.190 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.180 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.180 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0036572
Disease: Seizures
Seizures 		0.150 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0036572
Disease: Seizures
Seizures 		0.150 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome 		0.140 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0424605
Disease: Developmental delay (disorder)
Developmental delay (disorder) 		0.110 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.110 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.110 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0683322
Disease: Mental impairment
Mental impairment 		0.110 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.100 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.100 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653

2018
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.100 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 CausalMutation CLINVAR GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects. 28377535

2017
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.100 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196

2017