Acute Lung Injury
About the Disease
Adult Respiratory Distress Syndrome, also known as acute respiratory distress syndrome, is related to critical covid-19 and pulmonary edema, and has symptoms including apnea, cheyne-stokes respiration and coughing. An important gene associated with Adult Respiratory Distress Syndrome is CXCL8 (C-X-C Motif Chemokine Ligand 8), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Iron and Ibuprofen have been mentioned in the context of this disorder. Affiliated tissues include Lung, and related phenotypes are respiratory failure and tachypnea
Common Targets / Biomarkers
G11001 | Heat shock protein 90 (nonspecified subtype) | P5760 | G121504 | G4615 | G5196 | G7297 | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | Protein Kinase B (PKB/Akt) (nonspecified subtype) | G3551 | G10800 | G5159 | G5023 | G1734 | G4758 | Nuclear factor of activated T-cells (nonspecified subtype) | Chemokine CXC receptor (nonspecified subtype) | G1950 | G1432 | G5468 | G5578 | G59341 | G51684 | G4217 | G2908 | G9817 | G3383 | G3156 | G613 | G6439 | Chymotrypsin (nonspecified subtype) | G9429 | G10846 | Histone H3 (nonspecified subtype) | G929 | G2357 | G2152 | G54165 | G949 | G5743 | alpha-Adrenoceptor (nonspecified subtype) | G3776 | G5610 | Neurotrophic Factor (nonspecified subtype) | G729230 | P6884 | G1153 | G2260 | G9356 | G7189 | G2147 | G285 | G3630 | P24881 | G462 | G2532 | G7421 | G259292 | G6403 | G3480 | Adenylate Cyclase (nonspecified subtype) | G51135 | G26273 | G9971 | G1647 | G3586 | P6278 | G9376 | G4193 | G7225 | G29108 | G11251 | Interferon alpha/beta Receptor (nonspecified subtype) | G11156 | G5657 | G3553 | G796 | Trypsin (nonspecified subtype) | G7422 | G3569 | G4153 | Elastase (nonspecified subtype) | Serine protease (nonspecified subtype) | Caspase (nonspecified subtype) | G4843 | P6348 | G5138 | G5156 | G1230 | G1080 | G50508 | G2358 | G3717 | G9040 | P13475 | G1234 | G7428 | G623 | G9201 | G3718 | G10135 | G3082 | G355 | G3716 | P6058 | G4282 | G3576 | G407048 | G340061 | G240 | P24924 | G3146 | Nitric oxide synthase (NOS) (nonspecified subtype) | G554251 | G407049 | G3654 | G7132 | G3815 | G25 | alpha-Amylase (nonspecified subtype) | G7040 | G7124 | NADPH Oxidase (nonspecified subtype) | G5172 | P29419 | G710 | G4048 | G5434 | G2904 | G7099 | G9588 | G5266 | G4353 | G387 | G7056 | G11318 | G382 | G23643 | G3091 | TLR4/MD-2 complex | P5859 | G4194 | G6401 | G5478 | P16683 | Monoamine oxidase (MAO) (nonspecified subtype) | G115004 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | G1436 | G2993 | G624 | G1991 | G4780
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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 | 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| 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, 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| 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 | 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