Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2675496
Disease: Retinitis Pigmentosa 46
Retinitis Pigmentosa 46
0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C2675496
Disease: Retinitis Pigmentosa 46
Retinitis Pigmentosa 46
0.700 Biomarker disease CTD_human
CUI: C2675496
Disease: Retinitis Pigmentosa 46
Retinitis Pigmentosa 46
0.700 GeneticVariation disease UNIPROT Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle. 18806796 2008
CUI: C2675496
Disease: Retinitis Pigmentosa 46
Retinitis Pigmentosa 46
0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C2675496
Disease: Retinitis Pigmentosa 46
Retinitis Pigmentosa 46
0.700 CausalMutation disease CLINVAR
CUI: C2675496
Disease: Retinitis Pigmentosa 46
Retinitis Pigmentosa 46
0.700 Biomarker disease GENOMICS_ENGLAND Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle. 18806796 2008
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.510 Biomarker disease CTD_human Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle. 18806796 2008
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.510 Biomarker disease GENOMICS_ENGLAND
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.510 GeneticVariation disease LHGDN Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle. 18806796 2008
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.300 Biomarker disease CTD_human A gene expression signature of acquired chemoresistance to cisplatin and fluorouracil combination chemotherapy in gastric cancer patients. 21364753 2011
CUI: C1708349
Disease: Hereditary Diffuse Gastric Cancer
Hereditary Diffuse Gastric Cancer
0.300 Biomarker disease CTD_human A gene expression signature of acquired chemoresistance to cisplatin and fluorouracil combination chemotherapy in gastric cancer patients. 21364753 2011
Diabetes Mellitus, Non-Insulin-Dependent
0.100 Biomarker disease HPO
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.100 Biomarker disease HPO
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
0.100 Biomarker disease HPO
Sensorineural Hearing Loss (disorder)
0.100 Biomarker disease HPO
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.100 Biomarker disease HPO
CUI: C0020619
Disease: Hypogonadism
Hypogonadism
0.100 Biomarker disease HPO
CUI: C0022578
Disease: Keratoconus
Keratoconus
0.100 Biomarker disease HPO
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.100 Biomarker disease HPO
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease HPO
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
0.100 Biomarker disease HPO
CUI: C0086543
Disease: Cataract
Cataract
0.100 Biomarker disease HPO
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
0.100 Biomarker disease HPO
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
0.100 Biomarker disease HPO
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.010 Biomarker disease BEFREE Genetic analyses showed that IDH genes (IDH1, IDH2, IDH3A, IDH3B) and ACO genes (ACO1, ACO2) were not associated with BD. 26782057 2016