COX2, cytochrome c oxidase subunit II, 4513

N. diseases: 875; N. variants: 79
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency 		0.640 CausalMutation disease CLINVAR
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		0.520 Biomarker disease CTD_human
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.500 CausalMutation disease CLINVAR
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.500 GeneticVariation disease UNIPROT
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		0.470 Biomarker disease HPO
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.360 Biomarker disease HPO
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.200 Biomarker group HPO
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.160 Biomarker group HPO
CUI: C0015967
Disease: Fever
Fever 		0.160 Biomarker phenotype HPO
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.160 Biomarker disease HPO
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.150 Biomarker disease HPO
CUI: C0026848
Disease: Myopathy
Myopathy 		0.150 Biomarker group HPO
CUI: C0233794
Disease: Memory impairment
Memory impairment 		0.130 Biomarker phenotype HPO
CUI: C0003467
Disease: Anxiety
Anxiety 		0.120 Biomarker disease HPO
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.120 Biomarker group HPO
CUI: C0542476
Disease: Forgetful
Forgetful 		0.120 Biomarker phenotype HPO
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases 		0.120 CausalMutation group CLINVAR
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency 		0.120 Biomarker disease HPO
CUI: C0003123
Disease: Anorexia
Anorexia 		0.110 Biomarker disease HPO
CUI: C0003486
Disease: Aortic Aneurysm
Aortic Aneurysm 		0.110 Biomarker disease HPO
CUI: C0004134
Disease: Ataxia
Ataxia 		0.110 Biomarker phenotype HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.110 Biomarker disease HPO
CUI: C0013421
Disease: Dystonia
Dystonia 		0.110 Biomarker phenotype HPO
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.110 Biomarker disease HPO
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.110 Biomarker disease HPO