Diabetic Nephropathy
About the Disease
Microvascular Complications of Diabetes 2, also known as microvascular complications of diabetes, susceptibility to, 2, is related to microvascular complications of diabetes 3 and background diabetic retinopathy. An important gene associated with Microvascular Complications of Diabetes 2 is EPO (Erythropoietin). The drugs Mecobalamin and Hydroxocobalamin have been mentioned in the context of this disorder. Affiliated tissues include kidney, endothelial and retina.
Common Targets / Biomarkers
G1801 | G1636 | G105379399 | G3077 | P5755 | G6752 | G83596 | G8817 | G2936 | G387082 | G23389 | G1124 | G3636 | G4306 | G221692 | G5142 | G2915 | G83440 | G5465 | G102724087 | P16092 | G4627 | G4780 | G64122 | G3597 | G7317 | Protein kinase C (nonspecified subtype) | G2350 | G9779 | G4804 | G10800 | G26074 | G9612 | G59272 | G3958 | G4192 | G4842 | G84942 | G284391 | G5651 | G3117 | G5159 | G6559 | G2864 | G3574 | G152687 | G121551 | G388507 | G7295 | G2053 | G2162 | G779 | G93035 | G79809 | G2475 | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | G4128 | G1902 | G1950 | G5321 | G693123 | G9212 | G4199 | CDK5/p25 | G7299 | G80704 | G51557 | G5174 | G10280 | G5578 | G11343 | G10320 | G9370 | G183 | Endothelin-Converting Enzymes (ECE) (nonspecified subtype) | G1268 | G5468 | G8883 | P12327 | G406928 | G407040 | G7442 | G142 | G846 | G57495 | G3479 | G1520 | DNA Topoisomerase II (nonspecified subtype) | G4217 | G3163 | G7224 | G9817 | G6352 | G5241 | G1020 | G3383 | G187 | G2645 | G7058 | G8660 | G54901 | G9039 | G84649 | G5742 | G89795 | G10786 | G23158 | G23411 | G1514 | G246175 | G5313 | G116085 | G1374 | G5137 | G221710 | G23607 | G3135 | ADP-Ribosyl Cyclase/cyclic ADP-Ribose Hydrolase (ADPRC) (nonspecified subtype) | G2022 | G10014 | G9429 | G2908 | G128869 | G375248 | G101929129 | G10628 | Transforming growth factor (nonspecified subtype) | G4158 | G43 | G6339 | G442117 | G22986 | G50507 | G51085 | G3795 | G7111 | G9173 | G57572 | G22843 | G105375741 | G1803 | G4773 | G80310 | G8856 | G1490 | G841 | G6510 | G6648 | G4360 | G55504 | G729230 | G5467 | G54875 | G3605 | G100874095 | G9294 | G135 | Peroxisome Proliferator-Activated Receptors (PPAR) (nonspecified subtype) | G554 | G5743 | G57619 | G255738 | G27189 | G3630 | P24881 | G7039 | G231 | G8224 | G7046 | G2321 | G54206 | G5770 | G353500 | G5208 | G2876 | G5595 | G952 | G3854 | G7412 | G57466 | P38822 | G7052 | G7498 | G8801 | G3600 | G3643 | G1910 | G283284 | G3375 | G3689 | G4544 | G5243 | G2739 | G3614 | G83858 | P11113 | G2696 | G390260 | G7517 | G57099 | G9971 | G4524 | G219621 | G84310 | G2837 | G55693 | G4598 | G7421 | G3276 | G1903 | G2646 | G5795 | G1192 | G4159 | G122664 | G168090 | Mitogen-Activated Protein Kinase (nonspecified subtype) | G836 | G5287 | G6754 | G5054 | G57205 | G64478 | G114826 | G1278 | G5734 | Na+/K+-ATPase (nonspecified subtype) | G284459 | G93594 | G140 | G5601 | G4846 | G2729 | G9844 | G162466 | G79782 | G5340 | G7225 | G26751 | G102724768 | G5580 | G59307 | G3586 | G7010 | G84898 | Heme Oxygenase (HO) (nonspecified subtype) | G3791 | G100130698 | G11156 | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | G29128 | G7466 | G51586 | G26585 | G4311 | P10959 | Phospholipase A2, Cytosolic (nonspecified subtype) | G4313 | G7536 | G833 | G2569 | G150684 | G22852 | G53831 | G56670 | G3552 | G8654 | G9759 | G6833 | G10203 | G10560 | G9734 | G64241 | G646603 | Prostanoid TP receptor (nonspecified subtype) | G1649 | G823 | G29109 | G1147 | G7042 | G2690 | G6568 | G7422 | G2982 | G5933 | G3458 | G3553 | Transforming growth factor beta (nonspecified subtype) | G2153 | G23235 | G101929504 | G5153 | G101929523 | G4843 | G5741 | G54106 | G5579 | G5315 | G28996 | G9991 | G3569 | G2066 | G7296 | G22891 | G79400 | G53407 | G338440 | G2548 | G100288142 | G2846 | G5787 | G50508 | G2246 | G6523 | G185 | G2823 | G10320 | G26047 | G9379 | G5860 | G1234 | P5757 | G6513 | G4973 | G55512 | G335 | G5167 | G440584 | G5345 | G55604 | G6569 | G406938 | G7369 | G32 | G6755 | G10135 | G2879 | G27035 | Inosine 5'-monophosphate dehydrogenase (IMPDH) (nonspecified subtype) | G4744 | G1024 | G5602 | G3115 | G64061 | G4160 | G351 | P16740 | G4862 | G3565 | G3717 | G22925 | G55365 | G177 | G961 | G10855 | G57512 | G8542 | G3718 | G4481 | G1814 | G834 | G120425 | G348 | G186 | G2069 | G3716 | G1889 | G22807 | G10168 | G3146 | G4363 | G79068 | P24924 | G4036 | G7941 | G114548 | G56606 | G3576 | G6347 | P6058 | G51185 | Nitric oxide synthase (NOS) (nonspecified subtype) | G3596 | P5754 | G2740 | G64770 | G1672 | G2764 | G596 | G2149 | G9896 | G29922 | G7515 | G55148 | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | G105370003 | G6514 | G162989 | G1585 | G5305 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | alpha-Amylase (nonspecified subtype) | G23564 | G8764 | G10665 | G407051 | G101927438 | G3606 | G50807 | NADPH Oxidase (nonspecified subtype) | G7043 | G7220 | G7804 | G5581 | G105378977 | G3815 | G23171 | G290 | G3162 | P10999 | G6331 | Mitogen-activated protein kinase (JNK) (nonspecified subtype) | G102723341 | G6934 | G5136 | G768206 | G5972 | G137964 | G8639 | G1286 | G80772 | G90134 | Mitogen-activated protein kinase p38 (MAPK p38) (nonspecified subtype) | G387 | G6647 | G7040 | G23643 | Superoxide dismutase (SOD) (nonspecified subtype) | G9770 | G1215 | Vasopressin V1 Receptor (nonspecified subtype) | G7809 | G84265 | G54346 | G7099 | G5144 | G7351 | G2621 | Phosphodiesterase (nonspecified subtype) | G7568 | G10413 | Glutathione peroxidase (nonspecified subtype) | G401237 | G1909 | G2642 | G3091 | G3708 | G80776 | G9718 | P5767 | Transforming growth factor (TGF)-beta receptor (nonspecified subtype) | G847 | G29126 | G695 | G130271 | G3684 | G1535 | G55892 | G3655 | G3882 | G3931 | G23097 | G552 | G55867 | G9314 | G6524 | G7124 | G11000 | G151306 | G6916 | G113402 | G55328 | G9989 | G5820 | G102 | G57521 | G4591 | G5176 | G338557 | G6720 | G83639 | G90865 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | G10497 | G840 | G55811 | G1436 | G4256
Other Diseases
Diabetic Neuropathy | Diamond-Blackfan Anemia | Diarrhea | Diastrophic Dysplasia | DICER1 Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Diffuse Intrinsic Pontine Glioma | Diffuse Mesangial Sclerosis | Diffuse Palmoplantar Keratoderma | DiGeorge Syndrome | Discoid Lupus Erythematosus | Disseminated Intravascular Coagulation | Disseminated Superficial Actinic Porokeratosis | Distal Myopathy | Distal Myopathy 2 | Distal Spinal Muscular Atrophy | Diverticulitis | DNA Ligase IV Deficiency | DOCK8 Immunodeficiency Syndrome | Dominant Optic Atrophy | Donnai-Barrow Syndrome | Double Outlet Right Ventricle | Dowling-Degos Disease | Down Syndrome | DRESS Syndrome | Duane Retraction Syndrome | Dubin-Johnson Syndrome | Duchenne Muscular Dystrophy | Duodenal Atresia | Dupuytren Disease | Dwarfism | Dyggve-Melchior-Clausen Disease | Dysequilibrium Syndrome | Dysferlinopathy | Dysfibrinogenemia | Dyskeratosis Congenita | Dyslexia | Dyslipidemia | Dysmorphophobia | Dysplastic Nevus | Dysthymia | Dystonia | Dystonia Musculorum Deformans | Dystonia-parkinsonism, X-linked | Dystrophy, Cone-rod | Early Infantile Epileptic Encephalopathy | Early Infantile Epileptic Encephalopathy 1 | Early Infantile Epileptic Encephalopathy 13 | Early Infantile Epileptic Encephalopathy 28 | Early Infantile Epileptic Encephalopathy 4 | Eating Disorder | Ebstein Anomaly | Eccrine Porocarcinoma | Echinococcosis | Eclampsia | Ectodermal Dysplasia | Ectopia Lentis, Isolated, Autosomal Recessive | Ectrodactyly | Eczema | Ehlers-Danlos Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Eiken Syndrome | Ellis-Van Creveld Syndrome | Emery-Dreifuss Muscular Dystrophy | Empyema | Encephalitis | Encephalitis, Tick-borne | Encephalocele | Encephalopathy | Encephalopathy, Ethylmalonic | Encephalopathy, Glycine | Encephalopathy, Hepatic | Endocarditis | Endometrial Hyperplasia | Endometriosis | Endometritis | Endophthalmitis | Enhanced S-cone Syndrome | Enlarged Vestibular Aqueduct | Enterocolitis, Necrotizing | Eosinophilia | Eosinophilic Asthma | Ependymoma | Epicondylitis | Epidermal Nevus Syndrome | Epidermodysplasia Verruciformis | Epidermolysis Bullosa | Epidermolysis Bullosa Acquisita | Epidermolysis Bullosa Dystrophica | Epidermolysis Bullosa Simplex | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Epidermolysis Bullosa Simplex, Generalized | Epidermolysis Bullosa Simplex, Localized | Epidermolytic Hyperkeratosis | Epidermolytic Ichthyosis, Annular | Epidermolytic Palmoplantar Keratoderma | Epilepsy | Epilepsy Of Infancy With Migrating Focal Seizures | Epilepsy, Generalized | Epiphyseal Chondrodysplasia, Miura Type | Episodic Ataxia | Episodic Ataxia Type 1 | Episodic Ataxia Type 2 | Epithelial-myoepithelial Carcinoma | Epithelioid Hemangioma | Erdheim-Chester Disease | Erectile Dysfunction | Erysipelas | Erythema Multiforme | Erythema Nodosum | Erythematotelangiectatic Rosacea | Erythrokeratodermia Variabilis | Erythromelalgia | Erythropoietic Protoporphyria | Esophageal Adenocarcinoma | Esophageal Motility Disorders | Esophagitis | Essential Fructosuria | Esthesioneuroblastoma | Evans Syndrome | Exfoliative Dermatitis | Exocrine Pancreatic Insufficiency | Exostoses | Exotropia | Extramammary Paget's Disease | Fabry's Disease | Facioscapulohumeral Muscular Dystrophy | Facioscapulohumeral Muscular Dystrophy Type 1 | Facioscapulohumeral Muscular Dystrophy Type 2 | Fahr Disease | Familial Advanced Sleep Phase Syndrome | Familial Cerebral Amyloid Angiopathy | Familial Digital Arthropathy-brachydactyly | Familial Dysautonomia | Familial Episodic Pain Syndrome | Familial Exudative Vitreoretinopathy | Familial Glucocorticoid Deficiency | Familial Hemiplegic Migraine | Familial Hyperaldosteronism | Familial Hypertrophic Cardiomyopathy | Familial Hypobetalipoproteinemia | Familial Isolated Hyperparathyroidism | Familial Mediterranean Fever | Familial Partial Lipodystrophy | Familial Pheochromocytoma-paraganglioma | Familial Retinal Arterial Macroaneurysm | Familial Thoracic Aortic Aneurysm | Fanconi Anemia | Fanconi Syndrome | Farber Disease | Fascioliasis | Fatty Aldehyde Dehydrogenase Deficiency | Feingold Syndrome | Fetal Akinesia Deformation Sequence | Fetal Alcohol Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | FG Syndrome | Fibrillation, Atrial | Fibrodysplasia Ossificans Progressiva | Fibromuscular Dysplasia | Fibromyalgia | Fibronectin Glomerulopathy | Fibrosarcoma | Fibrosis | Filariasis | Focal Cortical Dysplasia Type 2 | Focal Dermal Hypoplasia | Focal Facial Dermal Dysplasia | Focal Segmental Glomerulosclerosis | Follicular Dendritic Cell Sarcoma | Fontaine Progeroid Syndrome | Fowler's Syndrome | Frank-ter Haar Syndrome | Frontometaphyseal Dysplasia | Frontotemporal Dementia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Fuchs Dystrophy | Fuchs Heterochromic Iridocyclitis | Fucosidosis | Fukuyama Congenital Muscular Dystrophy | Fundus Albipunctatus | Galactosemia | Galactosialidosis | Galloway-Mowat Syndrome | Gallstones | Ganglioglioma | Ganglioneuroma | Gangliosidosis | Gangliosidosis, GM1 | GAPO Syndrome | Gardner Syndrome | Gastric Atrophy | Gastritis | Gastritis, Atrophic | Gastroenteritis | Gastroenteritis, Eosinophilic | Gastrointestinal Disorders | Gastroschisis | GATA2 Deficiency | Gaucher Disease | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Genee-Wiedemann Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Generalized Epilepsy With Febrile Seizures Plus | Genitopatellar Syndrome | Gerodermia Osteodysplastica | Gerstmann-Straussler-Scheinker Syndrome | Gestational Trophoblastic Disease | Ghosal Syndrome | Giant Axonal Neuropathy | Giant Cell Arteritis | Giant Cell Glioblastoma | Gigantism | Gilbert Syndrome | Gingivitis | Gitelman Syndrome | Glanzmann Thrombasthenia | Glaucoma | Glaucoma, Congenital | Glaucomatocyclitic Crisis | Glioblastoma | Glioblastoma Multiforme | Glioma | Gliosarcoma | Globozoospermia | Glomerulonephritis | Glomerulonephritis, Membranoproliferative | Glomerulonephritis, Membranous | Glucagonoma | GLUT1 Deficiency Syndrome | Glutaric Aciduria Type 1 | Glutaric Aciduria Type 2 | Glutaric Aciduria Type 3 | Glutathione Synthetase Deficiency | Glycogen Storage Disease | Glycogen Storage Disease Type 0 | Glycogen Storage Disease Type 0, Muscle | Glycogen Storage Disease Type 1 | Glycogen Storage Disease Type 1a | Glycogen Storage Disease Type 1b | Glycogen Storage Disease Type 3 | Glycogen Storage Disease Type 4 | Glycogen Storage Disease Type 5 | Glycogen Storage Disease Type 6 | Glycogen Storage Disease Type 9 | GM2-gangliosidosis AB Variant | Gnathodiaphyseal Dysplasia | GNE Myopathy | Goiter | Goldenhar Syndrome | Gout | Graft-versus-host Disease | Granular Corneal Dystrophy | Granular Corneal Dystrophy Type 1 | Granuloma Annulare | Graves Disease | Gray Platelet Syndrome | Greenberg Dysplasia | Greig Cephalopolysyndactyly Syndrome | Growth Hormone Excess | Guanidinoacetate Methyltransferase Deficiency | Guillain-Barre Syndrome | Guttate Psoriasis | Gynecomastia | Gyrate Atrophy Of The Choroid And Retina | H Syndrome | Haim-Munk Syndrome | Hairy Cell Leukemia | Hamartoma | HANAC Syndrome | Hartnup Disease | Hartsfield Syndrome | Hashimoto Thyroiditis | Headache | Heart Block | Heart Failure | Heart Septal Defects | Heavy Chain Disease | Heimler Syndrome | HELLP Syndrome | Hemangioblastoma | Hemangioendothelioma | Hemangioma | Hemimegalencephaly | Hemochromatosis | Hemochromatosis Type 1 | Hemochromatosis Type 2 | Hemoglobinopathies | Hemolytic Anemia | Hemolytic Uremic Syndrome | Hemolytic Uremic Syndrome, Atypical | Hemophagocytic Lymphohistiocytosis | Hemophilia | Hemorrhage | Hemorrhagic Disorders | Hemorrhoids | Hemosiderosis | Hennekam Lymphangiectasia-lymphedema Syndrome | Hepatic Adenomatosis | Hepatic Steatosis | Hepatic Veno-occlusive Disease | Hepatitis | Hepatitis A | Hepatitis B, Chronic | Hepatitis C, Chronic | Hepatitis D | Hepatitis E | Hepatitis, Alcoholic | Hepatitis, Autoimmune | Hepatitis, Chronic | Hepatoblastoma | Hepatopulmonary Syndrome | Hepatorenal Syndrome | Hereditary Coproporphyria | Hereditary Elliptocytosis | Hereditary Folate Malabsorption | Hereditary Hemorrhagic Telangiectasia | Hereditary Hemorrhagic Telangiectasia Type 2 | Hereditary Mixed Polyposis Syndrome | Hereditary Multiple Exostoses | Hereditary Neuropathy With Liability To Pressure Palsies | Hereditary Pyropoikilocytosis | Hereditary Sensory And Autonomic Neuropathy | Hereditary Sensory Neuropathy Type 1 | Hereditary Spastic Paraplegia | Hereditary Spherocytosis | Hereditary Xerocytosis | Hermansky-Pudlak Syndrome | Hernia, Inguinal | Herpes Genitalis | Herpes Simplex Dermatitis | Heterotopic Ossification | HIBCH Deficiency | Hidradenitis | Hidradenitis Suppurativa | High Molecular Weight Kininogen Deficiency | Histiocytic Sarcoma | Histiocytosis | Hodgkin Lymphoma | Holoprosencephaly | Holt-Oram Syndrome | Homocystinuria | Hoyeraal-Hreidarsson Syndrome | Huntington's Disease | Huntington's Disease-like 2 | HUPRA Syndrome | Hydrocephalus | Hydrocephalus, Normal Pressure | Hydrolethalus Syndrome | Hydronephrosis | Hydrops Fetalis | Hyper IgE Syndrome | Hyperacusis | Hyperammonemia | Hyperandrogenemia | Hyperbilirubinemia, Neonatal | Hypercalcemia | Hypercalciuria | Hypercholesterolemia | Hypercholesterolemia, Familial | Hyperekplexia | Hypereosinophilic Syndrome | Hyperferritinemia-cataract Syndrome | Hyperglycemia | Hyperhomocysteinemia | Hyperinsulinemia | Hyperinsulinemic Hypoglycemia | Hyperinsulinism-hyperammonemia Syndrome | Hyperkeratosis | Hyperlipidemia | Hyperlipidemia Type V | Hyperlipidemia, Familial Combined | Hypermethioninemia | Hypermetropia | Hyperostosis | Hyperoxaluria | Hyperparathyroidism | Hyperparathyroidism, Primary | Hyperparathyroidism, Secondary | Hyperparathyroidism-jaw Tumor Syndrome | Hyperphenylalaninemia | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Hyperprolactinemia | Hypersensitivity | Hypersensitivity Pneumonitis | Hypersomnia | Hypertelorism | Hypertension | Hypertension, Essential | Hypertension, Portal | Hypertension, Pulmonary | Hypertension, Renal | Hypertension, Renovascular | Hypertensive Nephropathy | Hypertensive Retinopathy | Hyperthermia, Malignant | Hyperthyroidism | Hypertriglyceridemia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2
