Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 GeneticVariation disease BEFREE Recently, an association between a CA-repeat in the GABRA 3 gene and bipolar disorder had been reported. 15048654 2004
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET Recently, an association between a CA-repeat in the GABRA 3 gene and bipolar disorder had been reported. 15048654 2004
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET Moreover, the localization of the alpha3 subunit GABA receptor GABRA3 gene on the Xq28, a region of interest in certain forms of bipolar illness, suggests that GABRA3 may be a candidate gene in BPAD. 11840313 2002
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET The localization of the alpha3 subunit GABA receptor (GABRA3) gene in Xq28, a region of interest for BPAD suggests that GABRA3 may be a relevant candidate gene. 11602034 2001
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease BEFREE The localization of the alpha3 subunit GABA receptor (GABRA3) gene in Xq28, a region of interest for BPAD suggests that GABRA3 may be a relevant candidate gene. 11602034 2001
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET Lack of association between manic-depressive illness and a highly polymorphic marker from GABRA3 gene. 8546157 1995
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 GeneticVariation disease BEFREE Lack of association between manic-depressive illness and a highly polymorphic marker from GABRA3 gene. 8546157 1995
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.330 Biomarker disease PSYGENET X-linked manic depression and other psychiatric disorders have been mapped to this region, and thus GABRA3 is a potential candidate gene for these disorders. 2574000 1989
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.300 Biomarker disease PSYGENET This work suggests that GABRA3 regulates a behavioral endophenotype of depression and establishes this gene as a viable new target for the study and treatment of human depression. 20512339 2010
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.300 Biomarker disease PSYGENET This work suggests that GABRA3 regulates a behavioral endophenotype of depression and establishes this gene as a viable new target for the study and treatment of human depression. 20512339 2010
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.300 Biomarker disease CTD_human GABA(A) receptor downregulation in brains of subjects with autism. 18821008 2009
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
Thyrotoxic periodic paralysis
0.300 SusceptibilityMutation disease ORPHANET Association of genetic variants in GABRA3 gene and thyrotoxic hypokalaemic periodic paralysis in Thai population. 17970773 2008
CUI: C0009806
Disease: Constipation
Constipation
0.100 Biomarker phenotype HPO
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.100 Biomarker disease HPO
CUI: C0020458
Disease: Hyperhidrosis disorder
Hyperhidrosis disorder
0.100 Biomarker phenotype HPO
CUI: C0020461
Disease: Hyperkalemia
Hyperkalemia
0.100 Biomarker phenotype HPO
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease HPO
CUI: C0030252
Disease: Palpitations
Palpitations
0.100 Biomarker phenotype HPO
CUI: C0034372
Disease: Quadriplegia
Quadriplegia
0.100 Biomarker disease HPO
CUI: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis
0.100 Biomarker phenotype HPO
CUI: C0035410
Disease: Rhabdomyolysis
Rhabdomyolysis
0.100 Biomarker phenotype HPO
CUI: C0037763
Disease: Spasm
Spasm
0.100 Biomarker phenotype HPO
CUI: C0040822
Disease: Tremor
Tremor
0.100 Biomarker phenotype HPO
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation
0.100 Biomarker disease HPO
CUI: C0080274
Disease: Urinary Retention
Urinary Retention
0.100 Biomarker phenotype HPO