Disease

Galactosemia

About the Disease
Galactosemia I, also known as galactosemia, is related to galactosemia iii and galactosemia ii, and has symptoms including diarrhea, vomiting and icterus. An important gene associated with Galactosemia I is GALT (Galactose-1-Phosphate Uridylyltransferase), and among its related pathways/superpathways are Metabolism and Glycosaminoglycan metabolism. The drugs Aspartic acid and N-Methylaspartate have been mentioned in the context of this disorder. Affiliated tissues include liver, eye and kidney, and related phenotypes are male infertility and food intolerance

Common Targets
GALE | AKR1B1 | GALM | GALK1 | GALT

疾病靶点研报
Galactosemia

Note: If you'd like to get a target analysis report for Galactosemia, 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 Galactosemia at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Eczema | Strabismus | Periventricular Nodular Heterotopia | Lymphoma, B-cell | Wolfram Syndrome | Osteomalacia | Hyperostosis | Inborn Errors Of Metabolism | Juvenile Hyaline Fibromatosis | Diabetes | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Nestor-Guillermo Progeria Syndrome | Sorsby Fundus Dystrophy | Varicocele | Headache | Nicolaides-Baraitser Syndrome | Leukemia-lymphoma, Adult T-cell | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Spastic Paraplegia Type 7 | Multiple Sclerosis, Secondary Progressive | Hepatitis | Cheilitis | Hepatic Adenomatosis | Charcot-Marie-Tooth Disease Type 4D | Peyronie's Disease | Skin Papilloma | Pulmonary Alveolar Microlithiasis | Thyrotoxic Periodic Paralysis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Phenylketonuria | Protein C Deficiency | Alkaptonuria | McLeod Syndrome | Optic Neuropathy, Anterior Ischemic | Tendinitis | Keratoconjunctivitis | Rolandic Epilepsy | Atherosclerosis | Glioblastoma | Retinopathy, Diabetic | Lattice Corneal Dystrophy Type 1 | Multicentric Carpotarsal Osteolysis Syndrome | Tardive Dyskinesia | Gestational Trophoblastic Disease | Hemochromatosis Type 2 | TARP Syndrome | Persistent Truncus Arteriosus | Diabetes Gestational | Retinitis Pigmentosa 3 | Trismus-pseudocamptodactyly Syndrome | Epidermolysis Bullosa Dystrophica | Guanidinoacetate Methyltransferase Deficiency | Congenital Primary Aphakia | Hidradenitis | Diabetes Insipidus | Nephrotic Syndrome Type 1 | Nephroblastoma | Enlarged Vestibular Aqueduct | Juvenile Myelomonocytic Leukemia | Shwachman-Bodian-Diamond Syndrome | Dyslexia | Cyst | Chondrodysplasia Punctata 2, X-linked Dominant | Pregnancy, Ectopic | Chanarin-Dorfman Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Dengue Hemorrhagic Fever | Onchocerciasis | Parapsoriasis | Schwannoma | Schamberg Disease | Ovarian Hyperstimulation Syndrome | Meningioma | Wieacker-Wolff Syndrome | Acute Coronary Syndrome | Lymphangioma | Spinocerebellar Ataxia Type 10 | Ehlers-Danlos Syndrome | HELLP Syndrome | Acne | Swine Influenza | IgA Deficiency | Diabetic Neuropathy | Osteopetrosis | Pneumococcal Meningitis | C3 Glomerulopathy | Smith-Magenis Syndrome | Hypertension, Portal | Infertility | Torticollis | Pseudohypoparathyroidism Type 1A | Exostoses | Vertigo | Schnitzler Syndrome | Hypermethioninemia | Melanoma, Uveal | Primary Cutaneous Amyloidosis | Pemphigoid | Macular Degeneration | Pitt-Hopkins Syndrome | Conjunctivitis | Gastroenteritis, Eosinophilic | Fatty Aldehyde Dehydrogenase Deficiency | Specific Granule Deficiency | Postpoliomyelitis Syndrome | Multiple Sclerosis | Scapuloperoneal Spinal Muscular Atrophy | Fontaine Progeroid Syndrome | Polycythemia Vera | Fragile X Syndrome | Lymphomatoid Granulomatosis | Dementia, Vascular | Anorchia | Palsy, Cerebral | Fanconi Syndrome | Autoimmune Polyendocrine Syndrome | Epidermolysis Bullosa Simplex, Generalized | Granuloma Annulare | Myoclonus | Dubin-Johnson Syndrome | Leukocyte Adhesion Deficiency Type 1 | Chondrodysplasia Punctata 1, X-linked Recessive | Wolff-Parkinson-White Syndrome | Cholestasis, Intrahepatic | Lassa Fever | Benign Familial Neonatal Convulsions | Mumps | Gout | Tyrosinemia Type 1 | Gray Platelet Syndrome | Endophthalmitis | Hepatopulmonary Syndrome | Glomerulonephritis, Membranoproliferative | Allergic Contact Dermatitis | Spinocerebellar Ataxia Type 6 | Optic Nerve Hypoplasia, Bilateral | Chorioretinitis | Congenital Tufting Enteropathy | Epidermodysplasia Verruciformis | Sjogren Syndrome | Congenital Poikiloderma | Spinocerebellar Ataxia Type 20 | Keratoconus | Multiple Sulfatase Deficiency | Melanoma, Malignant | Orthostatic Intolerance | Hereditary Coproporphyria | Long QT Syndrome Type 2 | Familial Dysautonomia | Arteriosclerosis | Urticaria | Optic Nerve Diseases | Best Macular Dystrophy | DEND Syndrome | Mastitis | Otopalatodigital Syndrome Type 2 | Multiple Hamartoma Syndrome | Cystitis | Angioimmunoblastic T-cell Lymphoma | Hydrocephalus, Normal Pressure | Pulmonary Stenosis | Pleomorphic Xanthoastrocytoma | Keratopathy | Primary Torsion Dystonia | Primary Progressive Aphasia | Sarcoma, Alveolar Soft Part | Hoyeraal-Hreidarsson Syndrome | Lymphoma, AIDS-related | Meningococcal Infections | Idiopathic Pulmonary Fibrosis | Acute Myeloid Leukemia | Chondrodysplasia Punctata | Blau Syndrome | Pericarditis | Molybdenum Cofactor Deficiency | Metabolic Diseases | Amelogenesis Imperfecta | Narcolepsy | Cystitis, Interstitial | Alopecia Totalis | Patent Ductus Arteriosus | Craniopharyngioma | Major Depression | Schuurs-Hoeijmakers Syndrome | Anorectal Fistula | Kohlschutter-Tonz Syndrome | Polycystic Kidney, Autosomal Dominant | Obsessive-compulsive Disorder | Hamartoma | Amelanotic Melanoma | Rotor Syndrome | Chronic Periodontitis | Metachromatic Leukodystrophy | Stroke | Sensorineural Hearing Loss | Azoospermia | Abetalipoproteinemia | Paraplegia | Chitayat Syndrome | Melanoma | Periodontitis | Lichen Planus | Nanophthalmos | CDKL5 Deficiency Disorder | Spondyloarthritis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Weill-Marchesani Syndrome | Retinitis Pigmentosa | Hyperparathyroidism, Secondary | Cutaneous T-cell Lymphoma | Osteochondroma | Adams-Oliver Syndrome | Erythema Multiforme | Cyclic Vomiting Syndrome | Superficial Spreading Melanoma | Panniculitis | Seizures | Granular Corneal Dystrophy | Loeys-Dietz Syndrome | Bladder Exstrophy | Osteogenesis Imperfecta Type III | McCune-Albright Syndrome | Corneal Dystrophies, Hereditary | Hypereosinophilic Syndrome | Polycystic Liver | Sponastrime Dysplasia | Chondrosarcoma | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Babesiosis | Duchenne Muscular Dystrophy | Renal Tubular Dysgenesis | Congenital Central Hypoventilation Syndrome | Thyroid Hormone Resistance | Tibial Muscular Dystrophy | Chromosome 17q21.31 Deletion Syndrome | Tyrosine Hydroxylase Deficiency | Chordoid Glioma | Adenylosuccinate Lyase Deficiency | Kearns-Sayre Syndrome | Histiocytosis | Prolymphocytic Leukemia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Autonomic Neuropathy | Stromal Corneal Dystrophy | Cataplexy | Systemic Mastocytosis | Aneurysm, Abdominal Aortic | Hypocalcemia | Thrombotic Microangiopathy | Double Outlet Right Ventricle | Waardenburg Syndrome | Pityriasis Rubra Pilaris | Hidradenitis Suppurativa | Growth Hormone Excess | Cardiomyopathy, Dilated, 1L | Lymphoma, Mantle Cell | Nephrosclerosis | Crohn's Disease | Retinopathy Of Prematurity | Schaaf-Yang Syndrome | Basan Syndrome | Liddle Syndrome | Congenital Adrenal Hyperplasia | Mucormycosis | Rash | Hermansky-Pudlak Syndrome | Autosomal Recessive Congenital Ichthyosis | Cholecystitis | Ectodermal Dysplasia | Polycystic Kidney, Autosomal Recessive | Congenital Hemolytic Anemia | Meningococcal Meningitis | Carotid Artery Disease | Acute Tubular Necrosis | Astigmatism | Chronic Lymphocytic Leukemia | Glycogen Storage Disease Type 6 | Chloridorrhea, Congenital | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Colitis, Collagenous | Liebenberg Syndrome | D-2-Hydroxyglutaric Aciduria | Donnai-Barrow Syndrome | Jalili Syndrome | Iron Deficiency Anemia | Spinocerebellar Ataxia Type 13 | Ectrodactyly | Chondromyxoid Fibroma | Vitamin A Deficiency | Hereditary Hemorrhagic Telangiectasia Type 2 | Congenital Hereditary Endothelial Dystrophy Type I | Sengers Syndrome | Pfeiffer Syndrome | Angioedema, Acquired | L-2-Hydroxyglutaric Aciduria | Craniofrontonasal Syndrome | Melanocytic Nevus | Preaxial Polydactyly | Pathological Gambling | Asthma, Exercise-induced | Empyema | Richter's Syndrome | Mitochondrial DNA Depletion Syndrome | Chylomicron Retention Disease | Renal Failure | Periodic Limb Movement Disorder | Cornelia De Lange Syndrome | Muscle Wasting | Bainbridge-Ropers Syndrome | Oligospermia | Hyperekplexia | Congenital Ichthyosiform Erythroderma | Odonto-onycho-dermal Dysplasia | Gallstones | Hyperbilirubinemia | Congenital Hereditary Endothelial Dystrophy Type II | Glycogen Storage Disease | Acute Generalized Exanthematous Pustulosis | Leukocyte Adhesion Deficiency | Neurofibromatosis Type 1 | Apparent Mineralocorticoid Excess Syndrome | Pantothenate Kinase-associated Neurodegeneration | Compartment Syndrome | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Autoimmune Autonomic Ganglionopathy | Synovitis | Pompe Disease | Cerebrotendinous Xanthomatosis | Saethre-Chotzen Syndrome | Osteoporosis-pseudoglioma Syndrome | Metanephric Adenoma | Erythropoietic Protoporphyria | Progressive Familial Intrahepatic Cholestasis Type 2 | Niemann-Pick Disease | Rosacea | Nicotine Dependence | Hyperphenylalaninemia | Vascular Calcification | Myotonia | COACH Syndrome | Hypoproteinemia, Hypercatabolic | MELAS Syndrome | Harlequin Ichthyosis | Lentigo | Pyloric Stenosis, Infantile Hypertrophic | Sarcoma, Ewing | Tylosis With Esophageal Cancer | Wiskott-Aldrich Syndrome | Distal Spinal Muscular Atrophy | Myelodysplasia | Corticobasal Syndrome | Sporadic Hemiplegic Migraine | Ganglioneuroma | Muir-Torre Syndrome | Nager Acrofacial Dysostosis | Conjunctivitis, Allergic | Acquired Partial Lipodystrophy | Amyotrophic Lateral Sclerosis, Juvenile | Aicardi-Goutieres Syndrome | Pyoderma Gangrenosum | Anterior Segment Dysgenesis | Gaucher Disease | Hemoglobinopathies | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Methemoglobinemia | Polymyalgia Rheumatica | Lymphoma Lymphoblastic | Miyoshi Myopathy | Spinal Muscular Atrophy | Hyper IgE Syndrome | Osteosclerosis | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Lymphedema | Pancreatitis | Congenital Mirror Movements | Syphilis | Large Granular Lymphocytic Leukemia | Cardiomyopathy, Hypertrophic | Arthritis | Dyskeratosis Congenita | Gastrointestinal Disorders | Takayasu's Arteritis | Tetraplegia | Hereditary Pyropoikilocytosis | Mabry Syndrome | Jaundice, Obstructive | Lattice Corneal Dystrophy | Meier-Gorlin Syndrome | Acromegaly | Micro Syndrome | Gastritis, Atrophic | Lung Diseases | Situs Inversus | Lymphangiomatosis | 3-methylglutaconic Aciduria Type IV | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Sleep Apnea | Polyomavirus Nephropathy | Language Disorders | Cleidocranial Dysplasia