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: 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: C4023528
Disease: Abnormality of skin morphology
Abnormality of skin morphology 		0.100 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C1854882
Disease: Absent speech
Absent speech 		0.100 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C1854882
Disease: Absent speech
Absent speech 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C4317146
Disease: Acid reflux
Acid reflux 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0004106
Disease: Astigmatism
Astigmatism 		0.100 CausalMutation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0004134
Disease: Ataxia
Ataxia 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		0.100 GeneticVariation CLINVAR

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: C0008489
Disease: Chorea
Chorea 		0.100 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0233844
Disease: Clumsiness
Clumsiness 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0009806
Disease: Constipation
Constipation 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0239137
Disease: Coxa valga
Coxa valga 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		0.100 GeneticVariation GWASCAT Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. 22610502

2012
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		0.100 GeneticVariation CLINVAR

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		0.100 CausalMutation CLINVAR

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: C1836830
Disease: Developmental regression
Developmental regression 		0.100 Biomarker HPO

Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		0.100 GeneticVariation CLINVAR

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