Disease

Lipid Storage Diseases

About the Disease
Lipid Storage Disease, also known as lipoidosis, is related to chanarin-dorfman syndrome and sphingolipidosis. An important gene associated with Lipid Storage Disease is PNPLA2 (Patatin Like Phospholipase Domain Containing 2), and among its related pathways/superpathways are Metabolism and Glucose / Energy Metabolism. The drugs Bezafibrate and Clofibric Acid have been mentioned in the context of this disorder. Affiliated tissues include brain, liver and bone marrow, and related phenotypes are liver/biliary system and homeostasis/metabolism

Common Targets
Tubulin | UGCG | KIT | PNPLA2 | ABHD5 | CYP27A1 | Sphingolipid delta(4)-desaturase (nonspecified subtype) | DEGS2 | DEGS1

疾病靶点研报
Lipid Storage Diseases

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

Other Diseases

Schizotypal Personality Disorder | Retinoblastoma | Spondylosis | Neuroblastoma | Paraplegia | Mountain Sickness | Congenital Dyserythropoietic Anemia Type 4 | Rhabdomyosarcoma | Retinitis Pigmentosa | Viral Meningitis | Hyperacusis | Alpha-mannosidosis | Herpes Genitalis | Acne | Erectile Dysfunction | Esophagitis | Partington Syndrome | Stargardt Disease | Dystrophy, Cone-rod | Rhabdomyosarcoma, Embryonal | Myasthenia | Arrhythmogenic Right Ventricular Cardiomyopathy | Chudley-McCullough Syndrome | Cutaneous Mastocytosis | Dermatomyositis | Encephalopathy, Hepatic | Myotonia | Canavan Disease | Melanocytic Nevus | Sarcosinemia | Peters-plus Syndrome | Muir-Torre Syndrome | Raine Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Spondylocostal Dysostosis | Camptocormia | Charcot-Marie-Tooth Disease | Panuveitis | Silver-Russell Syndrome | Brugada Syndrome 1 | Periodic Limb Movement Disorder | Onchocerciasis | Spinocerebellar Ataxia Type 40 | Heavy Chain Disease | Sleep Apnea, Central | Colitis | Hyper IgE Syndrome | Wagner Disease | Borjeson-Forssman-Lehmann Syndrome | Craniofacial Dysostosis | Juvenile Myoclonic Epilepsy | Familial Advanced Sleep Phase Syndrome | Bruck Syndrome | Emery-Dreifuss Muscular Dystrophy | Keratocystic Odontogenic Tumor | VACTERL/VATER Association | Hypohidrotic Ectodermal Dysplasia, X-linked | Photosensitivity | Intellectual Disability, Autosomal Dominant 5 | Uremia | Gigantism | Meningioma, Benign | Myotonic Disorders | Split Hand-foot Malformation | Stroke, Hemorrhagic | Cellulitis | Optic Nerve Hypoplasia, Bilateral | Toxic Epidermal Necrolysis | Postaxial Polydactyly | Myositis | Pachyonychia Congenita | Stroke | Gnathodiaphyseal Dysplasia | Botulism | Brooke-Spiegler Syndrome | Waldenstrom Macroglobulinemia | DNA Ligase IV Deficiency | Hyperammonemia | Polyomavirus Nephropathy | Thrombosis | Oligoastrocytoma | Tyrosinemia Type 1 | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Molybdenum Cofactor Deficiency | Metanephric Adenoma | Microphthalmia | Potocki-Shaffer Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Neurotoxicity | Nanophthalmos | Pontocerebellar Hypoplasia Type 2 | Charcot-Marie-Tooth Disease Axonal Type 2N | Hemophilia | Syndactyly | Transcobalamin Deficiency | Tracheal Disorders | Retinitis Pigmentosa 3 | Dyslipidemia | Roberts Syndrome | Bartter Syndrome | Sclerosteosis 2 | Osteoporosis | Autosomal Recessive Spastic Paraplegia Type 54 | Dwarfism | Peripheral T-cell Lymphoma | Gastroschisis | Amish Infantile Epilepsy Syndrome | Lipodystrophy | Retinal Coloboma | Oculodentodigital Dysplasia | Pleurisy | Glycogen Storage Disease Type 0 | Porphyria, Variegate | Idiopathic Pulmonary Fibrosis | Osteogenesis Imperfecta Type IV | Aceruloplasminemia | Arts Syndrome | Hidradenitis | Costello Syndrome | Familial Retinal Arterial Macroaneurysm | Tendinopathy | Tuberculosis | Spinocerebellar Ataxia Type 10 | IgA Nephropathy | Stroke, Ischemic | Pseudohermaphroditism | Major Depression | Cole-Carpenter Syndrome | Porphyria, Acute Intermittent | Skin Carcinoma | Cholera | Non-epidermolytic Palmoplantar Keratoderma | Mucolipidosis Type IV | Hereditary Mixed Polyposis Syndrome | Infantile Spasm | Cluster Headache | COACH Syndrome | Agoraphobia | Optic Neuritis | Spondylometaphyseal Dysplasia | Usher Syndrome Type I | Hemochromatosis | Nephropathy | Craniofrontonasal Syndrome | Birt-Hogg-Dube Syndrome | Hepatorenal Syndrome | Chondrosarcoma | Hypertension, Essential | Liebenberg Syndrome | Diabetic Encephalopathy | Thalassemia | Gastric Atrophy | Metachromatic Leukodystrophy | Pierpont Syndrome | Osmotic Demyelination Syndrome | Rash | Mycosis Fungoides | Episodic Ataxia Type 2 | Gerodermia Osteodysplastica | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Lymphoproliferative Disorders | Pseudoachondroplasia | Osteochondrosis | Spasticity | Cerebral Amyloid Angiopathy | Blue Rubber Bleb Nevus Syndrome | Paroxysmal Kinesigenic Dyskinesia | Hypermethioninemia | Inflammatory Joint Disease | Encephalopathy | Birk-Barel Syndrome | Nicotine Addiction | Hyperinsulinemia | Lipid Storage Myopathy | Disseminated Intravascular Coagulation | Polyneuropathy | Cataract | Torticollis | Budd-Chiari Syndrome | Aplasia Cutis Congenita | Neurofibromatosis Type 1 | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Myelodysplasia | Thanatophoric Dysplasia Type 1 | Hepatitis D | Pneumonia, Viral | Polycystic Liver | Aspergillosis | Bietti Crystalline Dystrophy | Pituitary Disorders | Marshall-Smith Syndrome | H Syndrome | Neuroendocrine Cancer | Silicosis | Essential Fructosuria | Tenosynovial Giant Cell Tumor | Acrocallosal Syndrome | Tardive Dyskinesia | Vitamin D Deficiency | Congestive Heart Failure | Klinefelter Syndrome | Epidermolytic Hyperkeratosis | Bulimia Nervosa | Cranial Nerve Disease | Facioscapulohumeral Muscular Dystrophy | Renal-hepatic-pancreatic Dysplasia | Ischemia | Overactive Bladder | Contact Dermatitis | Meningeal Melanocytoma | McLeod Syndrome | Rift Valley Fever | Hamartoma | DiGeorge Syndrome | Hemimegalencephaly | Dyslexia | Chronic Lymphocytic Leukemia | Pneumonia, Mycoplasma | Gray Platelet Syndrome | Mohr-Tranebjaerg Syndrome | Primary Torsion Dystonia | Localized Scleroderma | Sandhoff Disease | Tinea | Narcolepsy | Spinocerebellar Ataxia Type 28 | Primary Sclerosing Cholangitis | Hartnup Disease | NGLY1 Deficiency | Tricho-hepato-enteric Syndrome | Waardenburg Syndrome Type 2 | Schindler Disease | Anorexia Nervosa | Open-angle Glaucoma | Ichthyosis Bullosa Of Siemens | Greig Cephalopolysyndactyly Syndrome | Carotid Artery Disease | Hyperandrogenemia | Early Infantile Epileptic Encephalopathy 4 | Iron Overload | Kaposiform Hemangioendothelioma | Chromosome 9q34.3 Deletion Syndrome | Presbycusis | Cholecystitis | Bullous Pemphigoid | Hemangioma | Diabetes Type 1 | Bronchitis, Chronic | Central Retinal Artery Occlusion | Lateral Meningocele Syndrome | Sotos Syndrome | Adrenomyeloneuropathy | L-2-Hydroxyglutaric Aciduria | Raynaud Phenomenon | POEMS Syndrome | Acute Chest Syndrome | Infantile Liver Failure Syndrome 1 | Asthma | Encephalitis, Tick-borne | Prostatitis | Thrombophilia | Charcot-Marie-Tooth Disease, Type 2 | Spondyloperipheral Dysplasia | Nephrotic Syndrome | Retinal Vasculitis | Persistent Truncus Arteriosus | Dementia | Albinism | Chromosome 17q21.31 Deletion Syndrome | Fundus Albipunctatus | Schwannomatosis | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Seizures-scoliosis-macrocephaly Syndrome | Stomatitis | Retinoschisis | Shwachman-Bodian-Diamond Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Hidradenitis Suppurativa | Malaria | Iron Metabolism Disorders | Cryoglobulinemia | Hyperkalemic Periodic Paralysis | Alagille Syndrome | Esthesioneuroblastoma | Imerslund-Grasbeck Syndrome | Hypocalcemia | Coenzyme Q10 Deficiency | Schistosomiasis Mansoni | Thin Basement Membrane Disease | Heterotopic Ossification | Tinea Versicolor | Leber Congenital Amaurosis | Mannosidase Deficiency Diseases | Hypoglycemia | Exfoliative Dermatitis | Borderline Personality Disorder | Ovarian Sex Cord-stromal Tumor | Choroiditis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Fibrodysplasia Ossificans Progressiva | Sialidosis | Prune Belly Syndrome | Farber Disease | Deafness, Dystonia, And Cerebral Hypomyelination | 3-methylglutaconic Aciduria Type IV | Primary Familial Brain Calcification | Cysticercosis | Pneumonia, Bacterial | Pelizaeus-Merzbacher Disease | Exocrine Pancreatic Insufficiency | Erythrokeratodermia Variabilis | Multiple System Atrophy | Myeloid Leukemia | Sarcoma, Ewing | Sarcoidosis, Pulmonary | Hyperinsulinemic Hypoglycemia | Meningococcal Infections | Glycogen Storage Disease Type 0, Muscle | Opisthorchiasis | Cancer, Bladder | Mood Disorder | Parvovirus B19 Infection | Cardiac Arrest | Trichorhinophalangeal Syndrome | Pancytopenia | Adult Polyglucosan Body Disease | Juvenile Hyaline Fibromatosis | Knobloch Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Loeys-Dietz Syndrome Type 4 | Glioblastoma | Pyoderma Gangrenosum | Ophthalmoplegia | Optic Atrophy 2 | Methemoglobinemia Type IV | Chronic Inflammatory Demyelinating Polyneuropathy | Patent Foramen Ovale | Influenza | Mastitis | Kindler Syndrome | Basan Syndrome | Adenocarcinoma | Hereditary Sensory Neuropathy Type 1 | Myhre Syndrome | Hypertension | Lewy Body Dementia | Cocaine-Related Disorders | Myosin Storage Myopathy | Leprosy | Congenital Myopathy | Muscle Wasting | Giant Cell Glioblastoma | SAPHO Syndrome | Fuchs Dystrophy | Aldosterone Deficiency | Adenylosuccinate Lyase Deficiency | Hyperparathyroidism, Primary | Juvenile Xanthogranuloma | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Rhabdoid Tumor | Salla Disease | Autosomal Recessive Congenital Ichthyosis | Osteogenesis Imperfecta Type III | DICER1 Syndrome | Holt-Oram Syndrome | Learning Disability | Pancreatitis | Porokeratosis | Transthyretin-related Amyloidosis | Keratopathy | Obesity | Alstrom Syndrome | Benign Hereditary Chorea | Currarino Syndrome | Plasma Cell Leukemia | Acute Motor Axonal Neuropathy | Gitelman Syndrome | Macrophage Activation Syndrome | Gaucher Disease | Xeroderma Pigmentosum | Adenosine Deaminase Deficiency | Epithelial-myoepithelial Carcinoma | Spondyloarthritis | Paternal Uniparental Disomy Of Chromosome 14 | Galloway-Mowat Syndrome | Pemphigus Vulgaris | Renal Tubular Acidosis | MELAS Syndrome | Senior-Loken Syndrome | Sclerosteosis | Angioedema, Hereditary | Hereditary Hemorrhagic Telangiectasia | Spinocerebellar Ataxia Type 7 | Spondylocarpotarsal Synostosis Syndrome | Retinal Telangiectasia | Genitopatellar Syndrome | Congenital Heart Defects | Takotsubo Cardiomyopathy | Corneal Dystrophies, Hereditary