Hypoalbuminemia

About the Disease
Analbuminemia, also known as analba, is related to lipid metabolism disorder and thalassemia. An important gene associated with Analbuminemia is ALB (Albumin), and among its related pathways/superpathways is FOXA2 and FOXA3 transcription factor networks. The drugs Esomeprazole and Norepinephrine have been mentioned in the context of this disorder. Affiliated tissues include heart, liver and kidney, and related phenotypes are hypoalbuminemia and fatigue

Common Targets
ANGPTL3 | ALB

Note: If you'd like to get a target analysis report for Hypoalbuminemia, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Hypoalbuminemia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

Other Diseases

Congenital Hereditary Endothelial Dystrophy Type II | Huntington's Disease-like 2 | Hidradenitis | Arthrogryposis | Neurofibrosarcoma | Urea Cycle Disorder | Gingivitis | Retinoschisis | Glutathione Synthetase Deficiency | Hypertension, Pulmonary | Acquired Partial Lipodystrophy | Hemangioblastoma | Meniere's Disease | Retinoblastoma | Hypertensive Nephropathy | Anti-glomerular Basement Membrane Disease | Meningeal Melanocytoma | Nephronophthisis | Cold Agglutinin Disease | IgA Nephropathy | Frontometaphyseal Dysplasia | Heterotopic Ossification | Farber Disease | Spinocerebellar Ataxia | Multiple Sulfatase Deficiency | Acute Chest Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Histiocytic Sarcoma | Neutrophilia | TARP Syndrome | Urofacial Syndrome | Prolymphocytic Leukemia | Exocrine Pancreatic Insufficiency | Pleural Tuberculosis | Coenzyme Q10 Deficiency | Glutaric Aciduria Type 1 | Mesothelioma, Malignant | Antithrombin III Deficiency | Colitis | Carcinoma, Merkel Cell | Patent Foramen Ovale | Panuveitis | Persistent Fetal Circulation | Optic Neuropathy, Anterior Ischemic | Chylothorax, Congenital | Asthma, Exercise-induced | Craniometaphyseal Dysplasia | Jaundice, Obstructive | Saul-Wilson Syndrome | Coronary Heart Disease | Trichothiodystrophy | Osteonecrosis | Actinomycetoma | Aplastic Anemia | Galactosialidosis | Schnyder Crystalline Corneal Dystrophy | Stargardt Disease | Vitamin A Deficiency | Plasmacytoma | Early Infantile Epileptic Encephalopathy 28 | Hypobetalipoproteinemias | Proteasome-associated Autoinflammatory Syndrome 2 | Syphilis | Cerebellar Ataxia, Cayman Type | Shprintzen-Goldberg Syndrome | CEDNIK Syndrome | Pulmonary Stenosis | Familial Cerebral Amyloid Angiopathy | Dystrophy, Cone-rod | Bronchiolitis | Papilledema | Autosomal Recessive Spastic Paraplegia Type 54 | Carbohydrate Metabolism Disorders | Blepharo-cheilo-odontic Syndrome | Congenital Adrenal Hyperplasia 1 | Sjogren Syndrome | Chondrodysplasia Punctata | Hypogonadism | Combined Malonic And Methylmalonic Acidemia | Usher Syndrome Type IIC | Lipid Metabolism Disorders | DICER1 Syndrome | Cystitis | Oculodentodigital Dysplasia | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Treacher Collins Syndrome | Sporadic Inclusion Body Myositis | Kallmann Syndrome | 3-M Syndrome | Tendinopathy | Encephalitis, Tick-borne | Chorea | Proopiomelanocortin Deficiency | Cutaneous T-cell Lymphoma | Polydactyly | Adenoma, Pleomorphic | Myotonic Disorders | Large Granular Lymphocytic Leukemia | Hypertension, Renovascular | Wagner Disease | Endophthalmitis | Dysmorphophobia | Hypodontia | Myelodysplasia | Metanephric Adenoma | Granular Corneal Dystrophy Type 1 | MELAS Syndrome | Muckle-Wells Syndrome | Joubert Syndrome 2 | Spinocerebellar Ataxia Type 3 | Nemaline Myopathy 8 | Pouchitis | Apraxia | IgA Deficiency | Carcinoma, Signet Ring Cell | Aarskog-Scott Syndrome | Acute Lymphocytic Leukemia | Neovascular Glaucoma | Acute Anterior Uveitis | Hairy Cell Leukemia | Micropenis | Hypermetropia | Succinic Semialdehyde Dehydrogenase Deficiency | Johanson-Blizzard Syndrome | GLUT1 Deficiency Syndrome | Renal Tubular Dysgenesis | Eczema | Ganglioneuroma | Cramp Fasciculation Syndrome | Pulmonary Veno-occlusive Disease | Spitzoid Melanoma | Meningioma | Insulinoma | Nephrotic Syndrome Type 1 | Dementia | Adenomyosis | Diamond-Blackfan Anemia | Warsaw Breakage Syndrome | Weill-Marchesani Syndrome | Congenital Myasthenic Syndrome | Pitt-Hopkins Syndrome | Spinocerebellar Ataxia Type 15 | Absence Epilepsy | H Syndrome | Osteosclerosis | Hemolytic Uremic Syndrome | Central Retinal Artery Occlusion | Senior-Loken Syndrome | Cutaneous Angiosarcoma | Hemorrhage | Ghosal Syndrome | Paraplegia | Neurotoxicity | Schamberg Disease | Osteonecrosis Of The Jaw | Glomerulonephritis, Membranous | Charcot-Marie-Tooth Disease, Type 1A | Blue Nevus | Dengue Shock Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Hypophosphatasia | Retinitis | X-linked Sideroblastic Anemia | Choriocarcinoma | Congenital Nystagmus | Familial Episodic Pain Syndrome | Chitayat Syndrome | Birk-Barel Syndrome | Gastritis, Atrophic | Kleine-Levin Syndrome | Erythema Nodosum | Lymphoma, AIDS-related | Jacobsen Syndrome | Varicocele | Spondylocarpotarsal Synostosis Syndrome | Waardenburg Syndrome Type 4 | Dysfibrinogenemia | Choroideremia | Retinopathy Of Prematurity | Primary Hyperoxaluria Type 3 | Tietze Syndrome | Goiter | ICF Syndrome | Meleda Disease | Myocarditis | Amyotrophic Lateral Sclerosis | Pulverulent Zonular Cataract | Pulmonary Alveolar Microlithiasis | Glaucoma | Angioimmunoblastic T-cell Lymphoma | Graft-versus-host Disease | Peritonitis | Achondrogenesis | Cleidocranial Dysplasia | Pseudoexfoliation Syndrome | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Fascioliasis | Chylomicron Retention Disease | Ependymoma | Creatine Deficiency Syndrome Due To AGAT Deficiency | Hemolytic Uremic Syndrome, Atypical | Corneal Dystrophies, Hereditary | Myofibrillar Myopathy | Major Depression | Liver Diseases | Osteogenesis Imperfecta Type IV | Alpha-mannosidosis | Chronic Inflammatory Demyelinating Polyneuropathy | Hepatoblastoma | Neuromyotonia | Stroke, Hemorrhagic | Borderline Personality Disorder | Pancytopenia | Insulin Resistance | Pelvic Inflammatory Disease | Castleman Disease | Withdrawal Syndrome | Pancreatitis, Chronic | Congenital Dyserythropoietic Anemia | WAGR Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Jawad Syndrome | Spondylolisthesis | Ocular Surface Squamous Neoplasia | Tenosynovial Giant Cell Tumor | Microcephaly, Seizures, And Developmental Delay | Porphyria, Acute Intermittent | Cholelithiasis | Atrioventricular Septal Defect | Campomelic Dysplasia | Poirier-Bienvenu Neurodevelopmental Syndrome | Acute Leukemia | Persistent Truncus Arteriosus | Spinal Muscular Atrophy Type 2 | Primary Hyperoxaluria | Swine Influenza | Osteopathia Striata With Cranial Sclerosis | Benign Familial Pemphigus | Trichorhinophalangeal Syndrome | Knobloch Syndrome | Tularemia | 3-methylglutaconic Aciduria | Imerslund-Grasbeck Syndrome | Leri Pleonosteosis | Chondrosarcoma | Emery-Dreifuss Muscular Dystrophy | Optic Nerve Hypoplasia, Bilateral | Snyder-Robinson Syndrome | Conjunctivitis, Allergic | Peters-plus Syndrome | Ovarian Sex Cord-stromal Tumor | Cholesteryl Ester Storage Disease | Currarino Syndrome | Nestor-Guillermo Progeria Syndrome | Diabetes Gestational | Optic Atrophy 2 | Sarcoidosis | Lentigo | Gigantism | Hepatic Steatosis | Coronary Artery Disease | Nemaline Myopathy 10 | Blepharospasm | Wiskott-Aldrich Syndrome | Aneurysm, Abdominal Aortic | Blue Rubber Bleb Nevus Syndrome | Ileitis | Metabolic Syndrome | Lymphangiomatosis | Biotinidase Deficiency | Myopia | CDKL5 Deficiency Disorder | Glycogen Storage Disease Type 1a | Rosacea | Postpartum Depression | Kaposiform Hemangioendothelioma | Polycystic Kidney, Autosomal Dominant | Keratopathy | Tinea Versicolor | Cervicitis | Hemorrhagic Disorders | Facioscapulohumeral Muscular Dystrophy Type 2 | Charcot-Marie-Tooth Disease | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Blepharophimosis Syndrome | Thrombosis | Chronic Granulomatous Disease, X-linked | Lymphoma, Follicular | Bicuspid Aortic Valve | Blomstrand Osteochondrodysplasia | Walker-Warburg Syndrome | Paget's Disease Of The Breast | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Empyema | Sengers Syndrome | Spinal Muscular Atrophy Type 3 | Clouston Hidrotic Ectodermal Dysplasia | Cranial Nerve Disease | Odonto-onycho-dermal Dysplasia | Alveolar Capillary Dysplasia | Spinal Muscular Atrophy | Erythropoietic Protoporphyria | Nephroblastoma | Urticaria | Malnutrition | Cole-Carpenter Syndrome | Orotic Aciduria | Leukemia-lymphoma, Adult T-cell | Familial Retinal Arterial Macroaneurysm | Heroin Dependence | Viral Meningitis | Vitreoretinal Degeneration, Snowflake Type | Hepatitis D | Ichthyosis | Pyruvate Dehydrogenase Deficiency | Bartsocas-Papas Syndrome | Glycogen Storage Disease Type 6 | Tibial Muscular Dystrophy | Liver Failure, Acute Infantile | Prediabetes | COACH Syndrome | Spasticity | Inflammatory Joint Disease | Idiopathic Pulmonary Fibrosis | Myosin Storage Myopathy | Lathosterolosis | Small Lymphocytic Lymphoma | Primary Carnitine Deficiency | Mitochondrial Myopathy | Impetigo | Multiple Sclerosis, Chronic Progressive | Retinitis Pigmentosa | VACTERL Association | X-linked Charcot-Marie-Tooth Disease | Benign Familial Neonatal Convulsions | Essential Fructosuria | Niemann-Pick Disease, Type C | Hermansky-Pudlak Syndrome | Early Infantile Epileptic Encephalopathy 1 | Sick Sinus Syndrome 1 | Rickets | Paronychia | Cervical Dystonia | Gastritis | Loeys-Dietz Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Stickler Syndrome | Juvenile Hyaline Fibromatosis | Primary Erythromelalgia | Episodic Ataxia | Hypohidrotic Ectodermal Dysplasia, X-linked | Intermittent Explosive Disorder | Addison Disease | Preaxial Polydactyly | Frank-ter Haar Syndrome | Thyroiditis, Autoimmune | Microphthalmia | Liddle Syndrome | REM Sleep Behavior Disorder | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Rhabdomyosarcoma, Alveolar | Neurofibroma | Dermatitis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Hyperparathyroidism-jaw Tumor Syndrome | Multiple Sclerosis, Primary Progressive | Neuroleptic Malignant Syndrome | Familial Isolated Hyperparathyroidism | Discoid Lupus Erythematosus | Gerodermia Osteodysplastica | Mumps | Mucolipidosis Type II | Yellow Fever | Pseudohypoaldosteronism | Trichotillomania | Seizures-scoliosis-macrocephaly Syndrome | Congenital Central Hypoventilation Syndrome | Primary Ovarian Insufficiency | Inflammatory Myopathy | Hepatitis, Chronic | Gynecomastia | Turner's Syndrome | Trismus-pseudocamptodactyly Syndrome | Infertility, Male | Neonatal Progeroid Syndrome | Atelosteogenesis Type 2 | Congenital Stromal Corneal Dystrophy | Nasodigitoacoustic Syndrome | Esophageal Adenocarcinoma | Wolfram Syndrome 2 | Charcot-Marie-Tooth Disease Type 2E | Cancer, Bladder | Wilson's Disease | Aphasia | Vitamin B12 Deficiency | Lassa Fever | Spinocerebellar Ataxia Type 7 | Basan Syndrome | Connective Tissue Disorders | Pterygium