* We recommend a score >= 0.08 for meaningful Gene-Disease associations

GeneID Gene_Symbol DisGeNet_diseaseID Disease_name DisGeNet score DisGeNet_sourceDB
6521SLC4A1C1704380Distal Renal Tubular Acidosis0.612637432073803BEFREE;HPO;ORPHANET;UNIPROT
6521SLC4A1C1969038RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA (disorder)0.6CTD_human;ORPHANET;UNIPROT
6521SLC4A1C2675212Spherocytosis, Type 40.48CTD_human;MGD;UNIPROT
6521SLC4A1C0001126Renal tubular acidosis0.422138026502723BEFREE;CTD_human;HPO;LHGDN
6521SLC4A1C0037889Hereditary spherocytosis0.409861453477037BEFREE;CTD_human;LHGDN;ORPHANET
6521SLC4A1C0002878Anemia, Hemolytic0.406839458850693BEFREE;CTD_human;HPO;LHGDN
6521SLC4A1C0013902Elliptocytosis, Hereditary0.403231208875927BEFREE;CTD_human;GAD;HPO
6521SLC4A1C1861453Pseudohyperkalemia Cardiff0.400549453568426BEFREE;ORPHANET;UNIPROT
6521SLC4A1C1864498RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE0.280549453568426BEFREE;CTD_human;MGD
6521SLC4A1C0024530Malaria0.209572371315507BEFREE;CTD_human;LHGDN
6521SLC4A1C1862323OVALOCYTOSIS, SOUTHEAST ASIAN0.204120901763196BEFREE;ORPHANET
6521SLC4A1C0027709Nephrocalcinosis0.20328236603324BEFREE;HPO;LHGDN
6521SLC4A1C0553720Spherocytosis0.202407028523288GAD;HPO
6521SLC4A1C2315100Pediatric failure to thrive0.200549453568426BEFREE;HPO
6521SLC4A1C0016663Pathological fracture0.2HPO
6521SLC4A1C0018939Hematological Disease0.2CTD_human
6521SLC4A1C0020598Hypocalcemia0.2HPO
6521SLC4A1C0022346Icterus0.2HPO
6521SLC4A1C0029442Osteomalacia0.2HPO
6521SLC4A1C0035579Rickets0.2HPO
6521SLC4A1C0038002Splenomegaly0.2HPO
6521SLC4A1C0206160Reticulocytosis0.2HPO
6521SLC4A1C0220981Metabolic acidosis0.2HPO
6521SLC4A1C0221409Anemia, hereditary spherocytic hemolytic0.2ORPHANET
6521SLC4A1C0231246Failure to gain weight0.2HPO
6521SLC4A1C0272051Xerocytosis0.2ORPHANET
6521SLC4A1C0311468Increased bilirubin level (finding)0.2HPO
6521SLC4A1C0427480Elliptocytosis found0.2HPO
6521SLC4A1C0677598Stomatocytosis Result0.2HPO
6521SLC4A1C1279412periodic paralysis (finding)0.2HPO
6521SLC4A1C1849478Increased red cell osmotic fragility0.2HPO
6521SLC4A1C1859778Postnatal growth retardation0.2HPO
6521SLC4A1C4020899Autosomal recessive predisposition0.2HPO
6521SLC4A1C4021553Periodic hypokalemic paresis0.2HPO
6521SLC4A1C4021768Abnormality of metabolism/homeostasis0.2HPO
6521SLC4A1C4280679Increased calcium level in kidney0.2HPO
6521SLC4A1C0032827Potassium Deficiency0.08RGD
6521SLC4A1C0042875Vitamin E Deficiency0.08RGD
6521SLC4A1C0015544Failure to Thrive0.00328236603323995BEFREE;LHGDN
6521SLC4A1C0019045Hemoglobinopathies0.00300763924902685BEFREE;LHGDN
6521SLC4A1C0001418Adenocarcinoma0.00273291246481375LHGDN
6521SLC4A1C0003130Anoxia0.00273291246481375LHGDN
6521SLC4A1C0005283beta Thalassemia0.00273291246481375LHGDN
6521SLC4A1C0022661Kidney Failure, Chronic0.00273291246481375LHGDN
6521SLC4A1C3714514Infection0.00273291246481375LHGDN
6521SLC4A1C0033117Priapism0.0026817553075011BEFREE;GAD
6521SLC4A1C0020503Hyperparathyroidism, Secondary0.002407028523288GAD
6521SLC4A1C0524910Hepatitis C, Chronic0.0010989071368524BEFREE
6521SLC4A1C0272048stomatocytic anemia0.0008241803526393BEFREE
6521SLC4A1C0002871Anemia0.0005494535684262BEFREE
6521SLC4A1C0002881Anemia, Hemolytic, Congenital0.0005494535684262BEFREE
6521SLC4A1C0024623Malignant neoplasm of stomach0.0005494535684262BEFREE
6521SLC4A1C0039730Thalassemia0.0005494535684262BEFREE
6521SLC4A1C0596263Carcinogenesis0.0005494535684262BEFREE
6521SLC4A1C0699791Stomach Carcinoma0.0005494535684262BEFREE
6521SLC4A1C2711227Steatohepatitis0.0005494535684262BEFREE
6521SLC4A1C3887638Failure to thrive in infant0.0005494535684262BEFREE
6521SLC4A1C0005806Blood Group Incompatibility0.0002747267842131BEFREE
6521SLC4A1C0009402Colorectal Carcinoma0.0002747267842131BEFREE
6521SLC4A1C0017636Glioblastoma0.0002747267842131BEFREE
6521SLC4A1C0017638Glioma0.0002747267842131BEFREE
6521SLC4A1C0018609Hartnup Disease0.0002747267842131BEFREE
6521SLC4A1C0019069Hemophilia A0.0002747267842131BEFREE
6521SLC4A1C0019214Hepatosplenomegaly0.0002747267842131BEFREE
6521SLC4A1C0020538Hypertensive disease0.0002747267842131BEFREE
6521SLC4A1C0022610Kernicterus0.0002747267842131BEFREE
6521SLC4A1C0022650Kidney Calculi0.0002747267842131BEFREE
6521SLC4A1C0023440Acute Erythroblastic Leukemia0.0002747267842131BEFREE
6521SLC4A1C0023895Liver diseases0.0002747267842131BEFREE
6521SLC4A1C0024534Malaria, Cerebral0.0002747267842131BEFREE
6521SLC4A1C0027765nervous system disorder0.0002747267842131BEFREE
6521SLC4A1C0033626Protein Deficiency0.0002747267842131BEFREE
6521SLC4A1C0151517Complete atrioventricular block0.0002747267842131BEFREE
6521SLC4A1C0239946Fibrosis, Liver0.0002747267842131BEFREE
6521SLC4A1C0275524Coinfection0.0002747267842131BEFREE
6521SLC4A1C0342208Multinodular goiter0.0002747267842131BEFREE
6521SLC4A1C0392525Nephrolithiasis0.0002747267842131BEFREE
6521SLC4A1C0684275Hemophilia, NOS0.0002747267842131BEFREE
6521SLC4A1C0687120Nephronophthisis0.0002747267842131BEFREE
6521SLC4A1C1306589Congenital dyserythropoietic anemia, type II0.0002747267842131BEFREE
6521SLC4A1C1527249Colorectal Cancer0.0002747267842131BEFREE
6521SLC4A1C1561643Chronic Kidney Diseases0.0002747267842131BEFREE
6521SLC4A1C1565489Renal Insufficiency0.0002747267842131BEFREE
6521SLC4A1C1861455STOMATOCYTOSIS I0.0002747267842131BEFREE