Disease

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

疾病靶点研报
Hypoalbuminemia

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.ai.

Other Diseases

Klippel-Feil Syndrome | Crigler-Najjar Syndrome | Charcot-Marie-Tooth Disease, Type 6 | Botulism | Colorectal Adenoma | Bardet-Biedl Syndrome | Teratozoospermia | Muscle Wasting | Oligospermia | Monilethrix | Cartilage Disorders | Extramammary Paget's Disease | Polymicrogyria | Gardner Syndrome | Parapsoriasis | Creatine Deficiency Syndrome | Obesity, Morbid | Galloway-Mowat Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Hypotension, Orthostatic | Dysequilibrium Syndrome | Malonyl-CoA Decarboxylase Deficiency | T-cell Lymphoma, Subcutaneous Panniculitis-like | Panniculitis | Paraganglioma, Carotid Body | Dwarfism | Schuurs-Hoeijmakers Syndrome | Liebenberg Syndrome | Nager Acrofacial Dysostosis | Rhabdoid Tumor | Glycogen Storage Disease Type 6 | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Corneal Ulcer | Filariasis | Dermatitis | Carney Triad | Autosomal Recessive Spastic Paraplegia Type 75 | Arthritis, Reactive | Paraganglioma | Aldosterone Deficiency | Hyperandrogenemia | Ventricular Septal Defect | Mohr-Tranebjaerg Syndrome | Dent Disease | Headache | Peters-plus Syndrome | Hydronephrosis | Yellow Fever | Reticular Dysgenesis | Tumoral Calcinosis | Adenocarcinoma | Pyruvate Kinase Deficiency | Spitz Nevus | Conjunctivitis, Allergic | Thrombocytopenia | Non-epidermolytic Palmoplantar Keratoderma | ADNP Syndrome | Angiosarcoma | Nicotine Addiction | Schizencephaly | Paracoccidioidomycosis | X-linked Myotubular Myopathy | Gitelman Syndrome | Hepatitis C, Chronic | Peeling Skin Syndrome, Acral Type | Chromosome 5q Deletion Syndrome | Schwartz-Jampel-Aberfeld Syndrome | Patent Ductus Arteriosus | Snyder-Robinson Syndrome | Osteogenesis Imperfecta Type III | Omenn Syndrome | Congenital Afibrinogenemia | Cold-induced Sweating Syndrome | Thanatophoric Dysplasia Type 1 | Sporadic Inclusion Body Myositis | Multicentric Carpotarsal Osteolysis Syndrome | Cocaine-Related Disorders | Schistosomiasis Mansoni | Lymphedema | Non-Hodgkin Lymphoma | Schwannomatosis | Acute Lymphocytic Leukemia | Hemoglobinopathies | Gastroenteritis | Seborrheic Dermatitis | Congenital Dyserythropoietic Anemia | Leiomyosarcoma | Camptocormia | Varicocele | Apparent Mineralocorticoid Excess Syndrome | Focal Cortical Dysplasia Type 2 | Otopalatodigital Syndrome Type 2 | Giant Cell Arteritis | Desbuquois Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Inflammatory Bowel Disease | Van Der Knaap Disease | Keratocystic Odontogenic Tumor | Turner's Syndrome | Tatton-Brown-Rahman Syndrome | Hyperlipidemia, Familial Combined | Heterotaxy | Renal Tubular Dysgenesis | Lipoma | Pseudohypoparathyroidism Type 1B | Astrocytoma, Anaplastic | Chylomicron Retention Disease | Gerodermia Osteodysplastica | Tylosis With Esophageal Cancer | Diabetes Insipidus | Early Infantile Epileptic Encephalopathy | Menetrier Disease | Rubeosis Iridis | Imerslund-Grasbeck Syndrome | Mucormycosis | Basal Ganglia Cerebrovascular Disease | Primary Cutaneous Amyloidosis | Dystonia | Androgenic Alopecia | Amish Infantile Epilepsy Syndrome | Swine Influenza | Strabismus | Pendred Syndrome | Carcinoma, Merkel Cell | Small Lymphocytic Lymphoma | Aneurysm, Abdominal Aortic | Pure Red Cell Aplasia | Centronuclear Myopathy | Mountain Sickness | Dowling-Degos Disease | Cri-du-chat Syndrome | Myoclonus | Bietti Crystalline Dystrophy | Tyrosinemia | Multiple Sclerosis, Secondary Progressive | Diabetes Type 2 | Vestibular Disease | Mood Disorder | Postaxial Polydactyly | Dysmorphophobia | Hemolytic Uremic Syndrome, Atypical | Immunoproliferative Disorders | Von Willebrand Disease | Oculopharyngeal Muscular Dystrophy | Transthyretin-related Amyloidosis | Pulmonary Stenosis | Brachial Plexus Neuropathy | Primary Lateral Sclerosis | Spina Bifida | Hypermethioninemia | Measles | Episodic Ataxia | Cabezas Syndrome | Spinocerebellar Ataxia Type 1 | Ovarian Sex Cord-stromal Tumor | FG Syndrome | Cancer, Brain | Fibromuscular Dysplasia | Charcot-Marie-Tooth Disease Type 4B1 | Paroxysmal Nocturnal Hemoglobinuria | Dengue Hemorrhagic Fever | Richter's Syndrome | Colitis, Microscopic | Graft-versus-host Disease | Amenorrhea | Sensory Neuropathy | Pulmonary Capillary Hemangiomatosis | Light Chain Amyloidosis | Aceruloplasminemia | Preaxial Polydactyly | VACTERL/VATER Association | Periodontitis | Hairy Cell Leukemia | Myelomeningocele | Chromosome 9q34.3 Deletion Syndrome | Plasma Cell Leukemia | Epidermolysis Bullosa | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Hemangioblastoma | Gestational Trophoblastic Disease | Borderline Personality Disorder | Pre-eclampsia | Treacher Collins Syndrome | Neuromuscular Disorders | Intestinal Hypomagnesemia 1 | Diabetes Gestational | Transient Bullous Dermolysis Of The Newborn | Leishmaniasis, Visceral | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Meckel-Gruber Syndrome | Knobloch Syndrome | Hyperglycemia | Pyruvate Carboxylase Deficiency Disease | Cutaneous Mastocytosis | Giant Axonal Neuropathy | Dermatomyositis | Porencephaly | Dementia | Neurocysticercosis | Behcet's Disease | Osteogenesis Imperfecta Type V | Heroin Dependence | Uveitis | Polyomavirus Nephropathy | Anodontia | Cutis Laxa | Ichthyosis Bullosa Of Siemens | Sleep Apnea, Obstructive | Cystinuria | Adenoma, Pituitary | Chronic Lymphocytic Leukemia | Erythromelalgia | Facioscapulohumeral Muscular Dystrophy | Pelizaeus-Merzbacher Disease | Low Phospholipid Associated Cholelithiasis | Pneumonia, Viral | Lymphangioma | Retinal Dystrophy, Early-onset Severe | Camurati-Engelmann Disease | Hyperinsulinemic Hypoglycemia | Atelosteogenesis Type 1 | Sorsby Fundus Dystrophy | Cryptococcal Meningitis | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Cramp Fasciculation Syndrome | Thrombotic Microangiopathy | Pontocerebellar Hypoplasia | Neurocutaneous Melanocytosis | Congenital Primary Aphakia | Thyroid Dyshormonogenesis | Homocystinuria | Cardiac Sarcoidosis | Chondroma | Familial Advanced Sleep Phase Syndrome | Wilson's Disease | Hidradenitis Suppurativa | Osteochondrosis | Myoclonic Atonic Epilepsy | Photosensitivity | Crohn's Disease | Chondrosarcoma | Megaloblastic Anemia | Pyloric Stenosis, Infantile Hypertrophic | Oculocutaneous Albinism Type 4 | Tetanus | Hypoparathyroidism | Hereditary Folate Malabsorption | Blue Rubber Bleb Nevus Syndrome | Crimean-Congo Hemorrhagic Fever | Hepatopulmonary Syndrome | Splenomegaly | Cerebellar Ataxia, Cayman Type | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Triple A Syndrome | Bronchiectasis | Multiple Sclerosis, Primary Progressive | Congenital Adrenal Hyperplasia 1 | Oligoasthenoteratozoospermia | Primary Hyperoxaluria | Hereditary Spastic Paraplegia | Smoldering Myeloma | Irritable Bowel Syndrome | Keratoconjunctivitis | Tibial Muscular Dystrophy | Rothmund-Thomson Syndrome | Anorectal Malformations | Motor Neuron Diseases | Persistent Truncus Arteriosus | Choriocarcinoma | Enhanced S-cone Syndrome | Chloridorrhea, Congenital | Exocrine Pancreatic Insufficiency | Pneumonia, Mycoplasma | Intermittent Explosive Disorder | Lysosomal Acid Lipase Deficiency | Chromosome 8q21.11 Deletion Syndrome | Isovaleric Acidemia | Gingivitis | Pineoblastoma | Sepiapterin Reductase Deficiency | Spinocerebellar Ataxia Type 42 | Angioedema, Acquired | Esotropia | Birt-Hogg-Dube Syndrome | Behavioral Variant Of Frontotemporal Dementia | Muckle-Wells Syndrome | Osteoarthritis | Ovarian Hyperstimulation Syndrome | Platelet Disorders | REM Sleep Behavior Disorder | Pneumonia, Bacterial | Lipodystrophy | Hydrocephalus, Normal Pressure | Leukocyte Adhesion Deficiency | Precocious Puberty | Epilepsy Of Infancy With Migrating Focal Seizures | Charcot-Marie-Tooth Disease Type 2D | Anuria | Pseudohypoparathyroidism Type 1A | Epidermolysis Bullosa Simplex, Generalized | Medulloblastoma | Hyperhomocysteinemia | Familial Hypertrophic Cardiomyopathy | Infantile Neuroaxonal Dystrophy | Multiple Hamartoma Syndrome | Arthritis, Gouty | Rhabdomyosarcoma, Embryonal | Sclerosing Cholangitis | DiGeorge Syndrome | Holt-Oram Syndrome | Limb Girdle Muscular Dystrophy | Erdheim-Chester Disease | Hyperuricemic Nephropathy, Familial Juvenile | Herpes Genitalis | Orthostatic Intolerance | Cystitis | Lipid Storage Myopathy | Hypersensitivity Pneumonitis | Hemophilia | Encephalocele | Spinocerebellar Ataxia Type 10 | Inborn Errors Of Metabolism | Neurofibroma, Plexiform | Myelitis, Transverse | Neurodermatitis | Fibrodysplasia Ossificans Progressiva | Ileitis | Depression | Waldenstrom Macroglobulinemia | Keratosis, Seborrheic | Glycogen Storage Disease | Costello Syndrome | Renal Tubular Acidosis | B-cell Prolymphocytic Leukemia | Familial Partial Lipodystrophy | Conn Syndrome | Syphilis | Liddle Syndrome | Glomerulonephritis | Dental Caries | Bronchitis | Methemoglobinemia Type IV | Coronary Restenosis | Haim-Munk Syndrome | Glutaric Aciduria Type 3 | Acral Lentiginous Melanoma | Hepatitis A | Wieacker-Wolff Syndrome | Ichthyosis | Waardenburg Syndrome Type 4 | Niemann-Pick Disease, Type C | Gliosarcoma | Mucolipidosis Type II | Hereditary Xerocytosis | Schizotypal Personality Disorder | Pouchitis | Addison Disease | Hypobetalipoproteinemias | Hyperlipidemia | Graves Disease | Antiphospholipid Syndrome | Vitiligo | Spitzoid Melanoma | Motion Sickness | Central Core Disease | Polymyalgia Rheumatica | Autoimmune Polyendocrine Syndrome | Carbohydrate Metabolism Disorders | Leukocyte Adhesion Deficiency Type 1 | Familial Digital Arthropathy-brachydactyly | Anencephaly | Congenital Nystagmus | GNE Myopathy | Epithelial-myoepithelial Carcinoma | Spinocerebellar Ataxia Type 16 | Fundus Albipunctatus | Nephronophthisis | Otitis Media | MELAS Syndrome | Presbyopia | Sarcoma, Alveolar Soft Part | Muir-Torre Syndrome | Hypohidrotic Ectodermal Dysplasia, X-linked | Epiphyseal Chondrodysplasia, Miura Type | Retinitis | Prostatitis | Tangier Disease | Sulfite Oxidase Deficiency | Mosaic Variegated Aneuploidy Syndrome 2 | Congenital Heart Defects | Localized Scleroderma | Greig Cephalopolysyndactyly Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Heavy Chain Disease | Insulin Resistance | Hepatitis E | POEMS Syndrome | Mixed Connective Tissue Disease | Mucolipidosis | Macular Corneal Dystrophy Type 1