Acute Kidney Injury
About the Disease
Acute Kidney Failure, also known as acute renal failure, is related to hemolytic-uremic syndrome and hemolytic uremic syndrome, atypical 1. An important gene associated with Acute Kidney Failure is MGAT3-AS1 (MGAT3 Antisense RNA 1), and among its related pathways/superpathways are Interleukin-4 and Interleukin-13 signaling and "Uricosurics Pathway, Pharmacodynamics". The drugs Desflurane and Racephedrine have been mentioned in the context of this disorder. Affiliated tissues include Bone and Adipose, and related phenotypes are homeostasis/metabolism and cardiovascular system
Common Targets / Biomarkers
G595 | G90865 | G1071 | G1773 | G100506047 | G5567 | G5052 | G121504 | G3355 | P16092 | G2150 | G5142 | G716 | G1269 | G105373053 | G3551 | G5465 | G4780 | G55869 | G2053 | G7157 | G727 | G655 | Lipoxygenase (nonspecified subtype) | P12327 | G1312 | G3163 | G142 | G2475 | G187 | G5468 | G9817 | G116085 | G282679 | G7124 | G23411 | Alkaline Phosphatase (ALP) (nonspecified subtype) | G259 | G5481 | G9173 | P5614 | G10059 | G5742 | Peroxisome Proliferator-Activated Receptors (PPAR) (nonspecified subtype) | G5467 | G1803 | G9429 | G3248 | G2876 | G3689 | P6884 | G2908 | Histone acetyltransferase (HAT) (nonspecified subtype) | G79648 | G59350 | G3934 | G51135 | G581 | G3630 | G7498 | G406958 | G81631 | G836 | Mitogen-Activated Protein Kinase (nonspecified subtype) | G5743 | G26751 | G4233 | K(ATP) Channel (nonspecified subtype) | G5243 | G7421 | G4781 | Heme Oxygenase (HO) (nonspecified subtype) | G7010 | G2538 | G1284 | G2166 | G1577 | Serine protease (nonspecified subtype) | G6615 | G4846 | G3586 | P11025 | Heat shock protein 70 (nonspecified subtype) | G4047 | G1956 | G130013 | G5970 | G1786 | G5104 | G7415 | G7422 | Histone deacetylase (nonspecified subtype) | P13475 | G23408 | G10135 | G2950 | G185 | G3082 | G3553 | G8542 | Hypoxia-Inducible Factor Prolyl Hydroxylase (nonspecified subtype) | G728 | G940 | G9934 | G2104 | G3569 | G4881 | G54583 | G4142 | Angiotensin receptor (AT) (nonspecified subtype) | G348 | G2149 | G23170 | G11103 | G596 | G2740 | Potassium Channels (nonspecified subtype) | G3576 | G1901 | G1524 | G8737 | G57591 | G11168 | G23387 | G3162 | G112398 | P6058 | G4353 | G1800 | G6647 | G4790 | G10013 | G8814 | G5478 | G3684 | G847 | G6524 | G55328 | P5859 | G5267 | G7099
Other Diseases
Acute Leukemia | Acute Lung Injury | Acute Lymphocytic Leukemia | Acute Motor Axonal Neuropathy | Acute Myeloid Leukemia | Adams-Oliver Syndrome | Addison Disease | Adenocarcinoma | Adenoid Cystic Carcinoma | Adenoma, Pituitary | Adenoma, Pleomorphic | Adenomatoid Tumor | Adenosine Deaminase 2 Deficiency | Adenosine Deaminase Deficiency | Adenylosuccinate Lyase Deficiency | ADNP Syndrome | Adrenal Insufficiency | Adrenoleukodystrophy, X-linked | Adrenomyeloneuropathy | Adult Polyglucosan Body Disease | Agammaglobulinemia | Agnathia-Otocephaly Complex | Agoraphobia | Agranulocytosis | Aicardi-Goutieres Syndrome | AIDS | AIDS Dementia Complex | Alagille Syndrome | Alazami Syndrome | Albinism | Alcoholism | Aldosterone Deficiency | Aldosterone Synthase Deficiency | Aldosteronism | Alexander Disease | Allan-Herndon-Dudley Syndrome | Allergic Contact Dermatitis | Alopecia | Alopecia Areata | Alopecia Totalis | Alpers Syndrome | Alpha-1 Antitrypsin Deficiency | Alpha-mannosidosis | Alpha-thalassemia Myelodysplasia Syndrome | Alstrom Syndrome | Alveolar Capillary Dysplasia | Alzheimer Disease, Late Onset | Amblyopia | Amelanotic Melanoma | Ameloblastic Carcinoma | Ameloblastoma | Amelogenesis Imperfecta | Amenorrhea | Amish Infantile Epilepsy Syndrome | Amyloidosis | Amyotrophic Lateral Sclerosis | Amyotrophic Lateral Sclerosis, Juvenile | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Anal Fissure | Analgesia | Androgenic Alopecia | Anemia | Anencephaly | Aneurysm, Abdominal Aortic | Aneurysm, Thoracic Aortic | Angelman Syndrome | Angina Pectoris | Angiodysplasia | Angioedema | Angioedema, Acquired | Angioedema, Hereditary | Angioimmunoblastic T-cell Lymphoma | Angiomyolipoma | Angiosarcoma | Angiosarcoma Of The Breast | Anodontia | Anorchia | Anorectal Fistula | Anorectal Malformations | Anorexia Nervosa | Anosmia, Congenital | Anovulation | Antenatal Bartter Syndrome Type 1 | Anterior Segment Dysgenesis | Anthrax | Anti-glomerular Basement Membrane Disease | Anti-NMDA Receptor Encephalitis | Antiphospholipid Syndrome | Antisocial Personality Disorder | Antisynthetase Syndrome | Antithrombin III Deficiency | Antley-Bixler Syndrome | Anuria | Anxiety Disorders | Apert Syndrome | Aphasia | Aplasia Cutis Congenita | Aplastic Anemia | Apparent Mineralocorticoid Excess Syndrome | Apraxia | Arrhythmogenic Right Ventricular Cardiomyopathy | Arterial Tortuosity Syndrome | Arteriosclerosis | Arteriovenous Malformations | Arthritis | Arthritis, Gouty | Arthritis, Psoriatic | Arthritis, Reactive | Arthrogryposis | Arthropathy | Arts Syndrome | Aspartylglycosaminuria | Asperger Syndrome | Aspergillosis | Asphyxia Neonatorum | Asplenia | Asthma | Asthma, Exercise-induced | Asthma, Nocturnal | Astigmatism | Astrocytoma | Astrocytoma, Anaplastic | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Ataxia-ocular Apraxia 2 | Atelosteogenesis Type 1 | Atelosteogenesis Type 2 | Atherosclerosis | Atopic Dermatitis | Atopy | Atrial Septal Defect | Atrioventricular Septal Defect | Auriculocondylar Syndrome | Autism | Autism Spectrum Disorders | Autoimmune Autonomic Ganglionopathy | Autoimmune Disease | Autoimmune Hemolytic Anemia | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Autoimmune Polyendocrine Syndrome | Autonomic Nervous System Disorders | Autonomic Neuropathy | Autosomal Recessive Bestrophinopathy | Autosomal Recessive Congenital Ichthyosis | Autosomal Recessive Spastic Paraplegia Type 35 | Autosomal Recessive Spastic Paraplegia Type 54 | Avellino Corneal Dystrophy | Axenfeld-Rieger Syndrome | Azoospermia | B-cell Chronic Lymphocytic Leukemia | B-cell Prolymphocytic Leukemia | Babesiosis | Bacterial Meningitis | Bainbridge-Ropers Syndrome | Barakat Syndrome | Bardet-Biedl Syndrome | Bare Lymphocyte Syndrome | Barrett Esophagus | Bartsocas-Papas Syndrome | Bartter Syndrome | Basal Cell Nevus Syndrome | Basal Ganglia Cerebrovascular Disease | Basal Ganglia Disease | Basal Ganglia Disease, Biotin-responsive | Basan Syndrome | Batten Disease | Beare-Stevenson Syndrome | Becker Muscular Dystrophy | Beckwith-Wiedemann Syndrome | Behavioral Variant Of Frontotemporal Dementia | Behcet's Disease | Benign Familial Infantile Seizures | Benign Familial Neonatal Convulsions | Benign Familial Pemphigus | Benign Hereditary Chorea | Benign Recurrent Intrahepatic Cholestasis 1 | Bernard-Soulier Syndrome | Best Macular Dystrophy | Beta-Propeller Protein-associated Neurodegeneration | Bethlem Myopathy | Bicuspid Aortic Valve | Bietti Crystalline Dystrophy | Binge Eating Disorder | Biotinidase Deficiency | Bipolar Disorder | Birk-Barel Syndrome | Birt-Hogg-Dube Syndrome | Bladder Exstrophy | Blastoma, Pleuropulmonary | Blastomycosis | Blau Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Blepharitis | Blepharo-cheilo-odontic Syndrome | Blepharoconjunctivitis | Blepharospasm | Blomstrand Osteochondrodysplasia | Blood Protein Disorders | Bloom Syndrome | Blue Nevus | Blue Rubber Bleb Nevus Syndrome | Bone Giant Cell Tumor | Bone Marrow Necrosis | Borderline Personality Disorder | Borjeson-Forssman-Lehmann Syndrome | Botulism | Brachial Plexus Neuropathy | Brachydactyly | Branchiootorenal Syndrome | Brenner Tumor | Bronchiectasis | Bronchiolitis | Bronchitis | Bronchitis, Chronic | Brooke-Spiegler Syndrome | Bruck Syndrome | Brugada Syndrome 1 | Budd-Chiari Syndrome | Bullous Pemphigoid | Burn-McKeown Syndrome | Bursitis | C3 Glomerulonephritis | C3 Glomerulopathy | Cabezas Syndrome | Calcium Pyrophosphate Deposition Disease | Campomelic Dysplasia | Camptocormia | Camurati-Engelmann Disease | Canavan Disease | Cancer, Bladder | Cancer, Brain | Cancer, Breast | Cancer, Colon | Cancer, Kidney | Cancer, Lung | Cancer, Prostate | Cancer, Skin | Cantu Syndrome | Carbohydrate Metabolism Disorders | Carbonic Anhydrase VA Deficiency | Carcinoid Syndrome | Carcinoid Tumor | Carcinoma In Situ | Carcinoma, Merkel Cell | Carcinoma, Signet Ring Cell | Carcinoma, Small Cell | Carcinoma, Squamous Cell | Carcinoma, Transitional Cell | Cardiac Arrest | Cardiac Sarcoidosis | Cardiofaciocutaneous Syndrome | Cardiomyopathy, Dilated, 1L | Cardiomyopathy, Hypertrophic | Cardiomyopathy, Restrictive | Cardiospondylocarpofacial Syndrome | Carey-Fineman-Ziter Syndrome | Carney Triad | Carney-Stratakis Syndrome | Carotid Artery Disease | Carpal Tunnel Syndrome | Cartilage Disorders | Castleman Disease | Cat Eye Syndrome | Cataplexy | Cataract | Cavitary Optic Disc Anomalies | CDKL5 Deficiency Disorder | CEDNIK Syndrome | Celiac Disease | Cellulitis | Cenani-Lenz Syndactyly Syndrome | Central Core Disease | Central Pain Syndrome | Central Retinal Artery Occlusion | Centronuclear Myopathy | Cerebellar Ataxia, Cayman Type | Cerebellofaciodental Syndrome | Cerebral Amyloid Angiopathy | Cerebral Cavernous Malformations | Cerebrotendinous Xanthomatosis | Cerebrovascular Disorders | Cervical Dystonia | Cervicitis | Chanarin-Dorfman Syndrome | Charcot-Marie-Tooth Disease | Charcot-Marie-Tooth Disease Axonal Type 2N | Charcot-Marie-Tooth Disease Type 2D | Charcot-Marie-Tooth Disease Type 2E | Charcot-Marie-Tooth Disease Type 2T | Charcot-Marie-Tooth Disease Type 3 | Charcot-Marie-Tooth Disease Type 4 | Charcot-Marie-Tooth Disease Type 4B1 | Charcot-Marie-Tooth Disease Type 4D | Charcot-Marie-Tooth Disease Type 4E | Charcot-Marie-Tooth Disease, Type 1A | Charcot-Marie-Tooth Disease, Type 2 | Charcot-Marie-Tooth Disease, Type 2A | Charcot-Marie-Tooth Disease, Type 2C | CHARGE Syndrome | Cheilitis | Chitayat Syndrome | Chloridorrhea, Congenital | Cholangiocarcinoma | Cholangitis | Cholecystitis | Cholelithiasis | Cholera | Cholestasis | Cholestasis, Intrahepatic | Cholesteryl Ester Storage Disease | Chondrodysplasia Punctata | Chondrodysplasia Punctata 1, X-linked Recessive | Chondrodysplasia Punctata 2, X-linked Dominant | Chondroma | Chondromyxoid Fibroma | Chondrosarcoma | CHOPS Syndrome | Chordoid Glioma | Chordoma | Chorea | Chorea-acanthocytosis | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Choriocarcinoma | Chorioretinitis | Choroideremia | Choroiditis | Christianson Syndrome | Chromosome 16p11.2 Deletion Syndrome | Chromosome 17q21.31 Deletion Syndrome | Chromosome 5q Deletion Syndrome | Chromosome 8q21.11 Deletion Syndrome | Chromosome 9q34.3 Deletion Syndrome | Chronic Beryllium Disease | Chronic Enteropathy Associated With SLCO2A1 Gene | Chronic Granulomatous Disease | Chronic Granulomatous Disease, X-linked | Chronic Idiopathic Myelofibrosis | Chronic Inflammatory Demyelinating Polyneuropathy | Chronic Kidney Disease | Chronic Leukemia | Chronic Lymphocytic Leukemia | Chronic Mucocutaneous Candidiasis | Chronic Myeloid Leukemia | Chronic Myelomonocytic Leukemia | Chronic Neutrophilic Leukemia | Chronic Periodontitis | Chronic Thromboembolic Pulmonary Hypertension | Chudley-McCullough Syndrome | Chylomicron Retention Disease | Chylothorax, Congenital | Cirrhosis | Citrullinemia | Cleidocranial Dysplasia | Clouston Hidrotic Ectodermal Dysplasia | Cluster Headache | COACH Syndrome | Cockayne Syndrome | Coenzyme Q10 Deficiency | Coffin-Lowry Syndrome | Coffin-Siris Syndrome | Cohen Syndrome | Cold Agglutinin Disease | Cold-induced Sweating Syndrome | Cole-Carpenter Syndrome | Colitis | Colitis, Collagenous | Colitis, Lymphocytic | Colitis, Microscopic | Coloboma | Colon Adenoma | Colorectal Adenoma | Coma | Combined Deficiency Of Factor V And Factor VIII | Combined Malonic And Methylmalonic Acidemia | Combined Pituitary Hormone Deficiency | Common Cold | Common Variable Immunodeficiency | Communication Disorders | Compartment Syndrome | Conduct Disorder | Cone Dystrophy | Congenital Absence Of Vas Deferens | Congenital Adrenal Hyperplasia | Congenital Adrenal Hyperplasia 1 | Congenital Afibrinogenemia | Congenital Aniridia | Congenital Bilateral Absence Of Vas Deferens | Congenital Bile Acid Synthesis Defect | Congenital Central Hypoventilation Syndrome | Congenital Diaphragmatic Hernia | Congenital Disorders Of Glycosylation | Congenital Disorders Of Glycosylation Type II | Congenital Dyserythropoietic Anemia | Congenital Dyserythropoietic Anemia Type 1 | Congenital Dyserythropoietic Anemia Type 4 | Congenital Dysfibrinogenemia | Congenital Fiber-type Disproportion Myopathy | Congenital Generalized Lipodystrophy | Congenital Heart Block | Congenital Heart Defects | Congenital Hemolytic Anemia
