Disease

Gaucher Disease

About the Disease
Gaucher's Disease, also known as gaucher disease, is related to gaucher disease, type ii and gaucher disease, type iii, and has symptoms including apnea, muscle rigidity and muscle spasticity. An important gene associated with Gaucher's Disease is GBA1 (Glucosylceramidase Beta 1), and among its related pathways/superpathways are Metabolism and Sphingolipid metabolism. The drugs Sofosbuvir and Ledipasvir have been mentioned in the context of this disorder. Affiliated tissues include spleen, liver and bone marrow, and related phenotypes are splenomegaly and hepatomegaly

Common Targets
CPVL | Histone deacetylase (nonspecified subtype) | Glucosidase (nonspecified subtype) | LYZ | GBA1 | MPHOSPH8 | Glycogen phosphorylase (nonspecified subtype) | LRRK2 | ASAH1 | UGCG | CHIT1 | Chaperone (nonspecified subtype) | CMYA5 | HLA-B | SLC5A4 | GUSB | PSAP | ZNF737 | HLA-DRB1 | HMMR | HLA-A | USH2A | ERN1 | Heat shock protein 70 (nonspecified subtype) | CACNA1A | PCDHB8 | GBA2 | GLB1 | MEST | DNAJC5 | GAA | NPC1 | GALC | TEAD3 | alpha-Mannosidase (nonspecified subtype) | GLA

疾病靶点研报
Gaucher Disease

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

Other Diseases

Pemphigus Foliaceus | Retinal Coloboma | Otitis Media | Optic Nerve Hypoplasia, Bilateral | Panniculitis | Reflex Epilepsy | Neuroectodermal Tumors, Primitive | Scapuloperoneal Myopathy, X-linked Dominant | Avian Influenza | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Gangliosidosis, GM1 | Mast Cell Leukemia | Delayed Sleep Phase Syndrome | Astrocytoma | Atrial Septal Defect | Whipple's Disease | Spinocerebellar Ataxia Type 3 | Pituitary Disorders | Klippel-Feil Syndrome | Retinal Telangiectasia | Myosin Storage Myopathy | Cancer, Lung | Netherton Syndrome | Retinopathy Of Prematurity | Hemolytic Uremic Syndrome, Atypical | Alveolar Capillary Dysplasia | Schnitzler Syndrome | Schuurs-Hoeijmakers Syndrome | Knobloch Syndrome | Azoospermia | Persistent Mullerian Duct Syndrome | Acute Chest Syndrome | Stiff-man Syndrome | Hepatitis E | Ureteropelvic Junction Obstruction | Osteogenesis Imperfecta Type III | Cryopyrin-associated Periodic Syndromes | Pain | Branchiootorenal Syndrome | Hyperhomocysteinemia | Hypophosphatasia | Thymoma, Malignant | Glycogen Storage Disease Type 1 | Bainbridge-Ropers Syndrome | Zimmermann-Laband Syndrome | Cardiac Sarcoidosis | Nemaline Myopathy | Focal Segmental Glomerulosclerosis | Osteopathia Striata With Cranial Sclerosis | Rubinstein-Taybi Syndrome | Cartilage Disorders | Episodic Ataxia | Ornithine Transcarbamylase Deficiency | Ulcerative Colitis | 3-methylcrotonyl-CoA Carboxylase Deficiency | Amenorrhea | Myelofibrosis | Urofacial Syndrome | CREST Syndrome | Borderline Personality Disorder | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Hereditary Multiple Exostoses | Hypospadias | Acute Leukemia | Inflammatory Bowel Disease | Fetal Alcohol Syndrome | Encephalopathy, Ethylmalonic | Choroideremia | Waardenburg Syndrome Type 1 | Echinococcosis | Distal Myopathy 2 | Loeys-Dietz Syndrome Type 4 | Deafness, Dystonia, And Cerebral Hypomyelination | Angiodysplasia | Vitreoretinal Degeneration, Snowflake Type | Bardet-Biedl Syndrome | Keratitis-ichthyosis-deafness Syndrome | Nijmegen Breakage Syndrome | Bullous Pemphigoid | Multiple Sclerosis, Relapsing-remitting | Bare Lymphocyte Syndrome | Usher Syndrome Type IIC | Bipolar Disorder | Aspergillosis | Exostoses | Currarino Syndrome | Juvenile Xanthogranuloma | H Syndrome | Lymphomatoid Granulomatosis | Dermatitis | Renal Tubular Dysgenesis | Epidermolytic Ichthyosis, Annular | Impetigo | Portal Vein Thrombosis | Facioscapulohumeral Muscular Dystrophy | Vertebrobasilar Insufficiency | Hyperlipidemia, Familial Combined | Mesothelioma, Malignant | Acromesomelic Dysplasia | Neurotoxicity | Agranulocytosis | Castleman Disease | Salla Disease | Limb Girdle Muscular Dystrophy | Lipoma | Postpoliomyelitis Syndrome | Hemolytic Uremic Syndrome | Congenital Tufting Enteropathy | Hidradenitis | Alstrom Syndrome | Primary Biliary Cholangitis | Schizophrenia, Paranoid | Blepharitis | Charcot-Marie-Tooth Disease Type 2T | Meier-Gorlin Syndrome | Antithrombin III Deficiency | Keratitis | Coronary Restenosis | Glaucoma, Congenital | Epidermolysis Bullosa Acquisita | Bronchiectasis | Sarcoma, Ewing | Craniosynostosis | McLeod Syndrome | Early Infantile Epileptic Encephalopathy 28 | Acanthosis Nigricans | Primary Torsion Dystonia | Tetraplegia | Oculocutaneous Albinism Type 4 | Familial Digital Arthropathy-brachydactyly | Auriculocondylar Syndrome | Galactosemia | Adrenomyeloneuropathy | Brooke-Spiegler Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Chronic Neutrophilic Leukemia | Adrenal Insufficiency | Addison Disease | Multiple Hamartoma Syndrome | Actinomycetoma | Menetrier Disease | Tyrosinemia Type 2 | Diamond-Blackfan Anemia | Sjogren Syndrome | Cerebral Amyloid Angiopathy | Congenital Heart Block | Oculodentodigital Dysplasia | Acrodermatitis | Hypertension | Pachyonychia Congenita | Intestinal Obstruction | Multifocal Motor Neuropathy | Wiskott-Aldrich Syndrome | Congenital Stationary Night Blindness | Paracoccidioidomycosis | Postpartum Depression | Nephropathy | Leukoencephalopathy, Progressive Multifocal | Fascioliasis | Coma | Congenital Stromal Corneal Dystrophy | Primary Cutaneous Amyloidosis | Persistent Hyperplastic Primary Vitreous | LRBA Deficiency | Achondrogenesis | Congenital Hemolytic Anemia | Meckel-Gruber Syndrome | Ectrodactyly | Stuve-Wiedemann Syndrome | Osteogenesis Imperfecta | Corneal Ulcer | Diastrophic Dysplasia | Angioedema, Hereditary | Meningitis | Endophthalmitis | Mandibuloacral Dysplasia With Type A Lipodystrophy | Thyroid Dyshormonogenesis | Nail Disorder, Nonsyndromic Congenital | Compartment Syndrome | Spinocerebellar Ataxia Type 31 | Leukemia-lymphoma, Adult T-cell | Fundus Albipunctatus | Melnick-Needles Syndrome | Renal Hypouricemia | Adenylosuccinate Lyase Deficiency | Venous Insufficiency | Chorea | Aldosterone Deficiency | Anthrax | Low Phospholipid Associated Cholelithiasis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Arteriovenous Malformations | Fucosidosis | Lathosterolosis | Congenital Disorders Of Glycosylation | Heart Failure | Hypercholesterolemia, Familial | Hyperacusis | Hereditary Neuropathy With Liability To Pressure Palsies | Mood Disorder | Spinocerebellar Ataxia Type 28 | Tremor | Congenital Adrenal Hyperplasia 1 | Dentinogenesis Imperfecta | Bladder Exstrophy | Seborrheic Dermatitis | Anencephaly | Periventricular Leukomalacia | Hypotension, Orthostatic | Polymicrogyria | Lichen Planus | Dysferlinopathy | Prune Belly Syndrome | Atelosteogenesis Type 1 | Tatton-Brown-Rahman Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Leishmaniasis, Cutaneous | Pleurisy | Restless Legs Syndrome | Christianson Syndrome | Pure Red Cell Aplasia | Loeys-Dietz Syndrome | Platelet Disorders | Presbycusis | Lymphoproliferative Disease, X-linked | Hashimoto Thyroiditis | Alpha-mannosidosis | Cervicitis | Dengue Hemorrhagic Fever | Tumoral Calcinosis | Xeroderma Pigmentosum Variant Type | Epidermodysplasia Verruciformis | Pregnancy, Ectopic | Nail-Patella Syndrome | Lewy Body Dementia | Renal Dysplasia | Hepatitis, Alcoholic | Stroke | Facioscapulohumeral Muscular Dystrophy Type 1 | Encephalitis | Jawad Syndrome | Narcolepsy | Sialidosis Type I | Asperger Syndrome | Vaginitis | Meningioma | Spondyloarthritis | Senior-Loken Syndrome | Gardner Syndrome | Retinal Dystrophy, Early-onset Severe | Thyroiditis, Autoimmune | Hereditary Pyropoikilocytosis | Dent Disease | Optic Atrophy 2 | Meesmann Corneal Dystrophy | Pathological Gambling | Galloway-Mowat Syndrome | Transcobalamin Deficiency | Hypopigmentation | Muir-Torre Syndrome | Pleomorphic Xanthoastrocytoma | Osteoporosis | Mucolipidosis Type II | Schistosomiasis Mansoni | Cirrhosis | Giant Cell Glioblastoma | T-cell Lymphoma, Subcutaneous Panniculitis-like | Influenza | Spinocerebellar Ataxia Type 27 | Monilethrix | Hyperostosis | Peritonitis | Spinocerebellar Ataxia Type 38 | Conjunctivitis | Ovarian Sex Cord-stromal Tumor | Cholangitis | Vitamin K Deficiency | Patent Foramen Ovale | Hypertensive Retinopathy | Prediabetes | DNA Ligase IV Deficiency | Prurigo Nodularis | Microphthalmia, Syndromic 7 | Chromosome 5q Deletion Syndrome | Kaposiform Hemangioendothelioma | Dwarfism | Megaloblastic Anemia | Diarrhea | Polymyositis | Absence Epilepsy | Palsy, Cerebral | Dupuytren Disease | Gerodermia Osteodysplastica | Connective Tissue Disorders | Nephritis, Interstitial | Hereditary Spherocytosis | Apraxia | Optic Neuritis | CHARGE Syndrome | Congenital Poikiloderma | Sickle Cell Anemia | Congenital Diaphragmatic Hernia | High Molecular Weight Kininogen Deficiency | Pheochromocytoma | Hyperuricemia | Paget's Disease Of The Breast | Dyslexia | Metabolic Syndrome | Kindler Syndrome | Fukuyama Congenital Muscular Dystrophy | Exocrine Pancreatic Insufficiency | Antiphospholipid Syndrome | Lupus Erythematosus | Acromegaly | Sporadic Hemiplegic Migraine | Thrombocytopenia | Reticular Dysgenesis | Cardiomyopathy, Peripartum | Spondylo-ocular Syndrome | Hereditary Mixed Polyposis Syndrome | Liver Diseases | Lattice Corneal Dystrophy | Lymphoma, Follicular | Dyggve-Melchior-Clausen Disease | Prolidase Deficiency | Shprintzen-Goldberg Syndrome | Glucagonoma | Urolithiasis | Congenital Heart Defects | Optic Nerve Diseases | Vitreoretinopathy, Proliferative | Intestinal Tuberculosis | Glycogen Storage Disease Type 5 | Stomatitis | Liver Failure | Cohen Syndrome | Leri-Weill Dyschondrosteosis | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Chromosome 16p11.2 Deletion Syndrome | Sclerosing Cholangitis | Adams-Oliver Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Tricho-hepato-enteric Syndrome | Glutaric Aciduria Type 1 | Presbyopia | Nephrotic Syndrome | Herpes Simplex Dermatitis | Retinitis Pigmentosa | Isovaleric Acidemia | DRESS Syndrome | Incontinentia Pigmenti | GATA2 Deficiency | Kabuki Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Kleine-Levin Syndrome | SAPHO Syndrome | Ischemia | Leiomyoma | Cancer, Kidney | Silicosis | Glycogen Storage Disease Type 6 | Infertility, Male | Juvenile Myoclonic Epilepsy | Onchocerciasis | Cannabis Abuse | Postaxial Polydactyly | Poikiloderma With Neutropenia | Beta-Propeller Protein-associated Neurodegeneration | Diffuse Palmoplantar Keratoderma | Crohn's Disease | Holt-Oram Syndrome | Graft-versus-host Disease | Choriocarcinoma | Preaxial Polydactyly | Thanatophoric Dysplasia | Hypoglycemia | Hemolytic Anemia | Neonatal Progeroid Syndrome | Retinoblastoma | Smith-Kingsmore Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Erdheim-Chester Disease | Canavan Disease | KBG Syndrome | Carey-Fineman-Ziter Syndrome | Birt-Hogg-Dube Syndrome | DiGeorge Syndrome | Hypodontia | Cardiospondylocarpofacial Syndrome | Coenzyme Q10 Deficiency | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Sarcoma, Endometrial Stromal | Hemorrhagic Disorders | Congenital Dyserythropoietic Anemia Type 4 | Glycogen Storage Disease Type 1b | Dementia | Hyperinsulinemia | Osteosclerosis | Liddle Syndrome | Peutz-Jeghers Syndrome