Disease

3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency

About the Disease
3-Hydroxy-3-Methylglutaryl-Coa Synthase-2 Deficiency, also known as 3-hydroxy-3-methylglutaryl-coa synthase deficiency, is related to hmg coa synthetase deficiency and hypertriglyceridemia 1, and has symptoms including diarrhea and vomiting. An important gene associated with 3-Hydroxy-3-Methylglutaryl-Coa Synthase-2 Deficiency is HMGCS2 (3-Hydroxy-3-Methylglutaryl-CoA Synthase 2). Affiliated tissues include liver and brain, and related phenotypes are hypoglycemia and seizure

Common Targets
HMGCS2 | HMGCL

疾病靶点研报
3-hydroxy-3-methylglutaryl-CoA synthase deficiency

Note: If you'd like to get a target analysis report for 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency, 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 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

Other Diseases

Aplasia Cutis Congenita | Frontometaphyseal Dysplasia | Focal Segmental Glomerulosclerosis | Migraine | Hereditary Hemorrhagic Telangiectasia Type 2 | Fukuyama Congenital Muscular Dystrophy | Hyperoxaluria | Camptocormia | Pulmonary Tuberculosis | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Multicentric Carpotarsal Osteolysis Syndrome | Perry Syndrome | Chondrodysplasia Punctata 2, X-linked Dominant | Angiodysplasia | Chloridorrhea, Congenital | Robinow Syndrome | Spinocerebellar Ataxia Type 38 | Placenta Previa | Pyruvate Dehydrogenase Deficiency | Oculocutaneous Albinism Type 2 | Restless Legs Syndrome | NDH Syndrome | Orotic Aciduria | Pearson Syndrome | Anthrax | Hashimoto Thyroiditis | Kallmann Syndrome | Ganglioneuroma | Pendred Syndrome | Neurofibromatosis | Sialidosis | Lactose Intolerance | Pernicious Anemia | Acne Vulgaris | Gliosarcoma | Chronic Enteropathy Associated With SLCO2A1 Gene | Primary Torsion Dystonia | Arthritis | Dystonia Musculorum Deformans | Creatine Deficiency Syndrome | Thrombocythemia, Essential | Epidermolytic Ichthyosis, Annular | Sporadic Inclusion Body Myositis | Hypospadias | Cranial Nerve Disease | Colitis, Microscopic | Gray Platelet Syndrome | Hemorrhoids | Temtamy Preaxial Brachydactyly Syndrome | Congenital Central Hypoventilation Syndrome | Lung Diseases | Acquired Partial Lipodystrophy | Camurati-Engelmann Disease | Glutaric Aciduria Type 2 | McKusick Type Metaphyseal Chondrodysplasia | Monilethrix | Wagner Disease | Epithelioid Hemangioma | Demyelinating Diseases | Tularemia | Tietze Syndrome | Abetalipoproteinemia | Cancer, Kidney | Pulmonary Capillary Hemangiomatosis | Hyperostosis | Pemphigus | Cherubism | Measles | Spinocerebellar Ataxia Type 2 | Lewy Body Dementia | Long QT Syndrome Type 1 | Paroxysmal Kinesigenic Dyskinesia | Niemann-Pick Disease | Leber Congenital Amaurosis | Methylmalonic Acidemia | Tracheal Disorders | Hypersensitivity Pneumonitis | Lymphangioleiomyomatosis | Proctitis | Congenital Diaphragmatic Hernia | Pseudohypoparathyroidism Type 2 | Enlarged Vestibular Aqueduct | Crigler-Najjar Syndrome | Seizures | Hyper IgE Syndrome | Chylomicron Retention Disease | Epidermolysis Bullosa Simplex | Huntington's Disease | Weill-Marchesani Syndrome | Milk Allergy | Kashin-Beck Disease | Infantile Spasm | Fibronectin Glomerulopathy | Herpes Genitalis | Glycogen Storage Disease Type 1a | Long QT Syndrome Type 3 | Norrie Disease | Autism | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Blastoma, Pleuropulmonary | Dyskeratosis Congenita | Focal Cortical Dysplasia Type 2 | Ellis-Van Creveld Syndrome | Acute Kidney Injury | Guanidinoacetate Methyltransferase Deficiency | Hyperkalemic Periodic Paralysis | Osmotic Demyelination Syndrome | Walker-Warburg Syndrome | Persistent Truncus Arteriosus | Diverticulitis | Autoimmune Polyendocrinopathy Syndrome Type I | Cohen Syndrome | Carbonic Anhydrase VA Deficiency | Hereditary Spherocytosis | Hemochromatosis | Hypotension, Orthostatic | Mesothelioma, Malignant | Anorectal Fistula | 3-methylcrotonyl-CoA Carboxylase Deficiency | L-2-Hydroxyglutaric Aciduria | Chorea | Neurocysticercosis | Astrocytoma | Dengue Shock Syndrome | Endometriosis | Waardenburg Syndrome Type 2E | Atopic Dermatitis | Stiff-man Syndrome | Hyperphenylalaninemia | Babesiosis | Schizencephaly | NGLY1 Deficiency | Kindler Syndrome | Rash | Myoclonic Atonic Epilepsy | Charcot-Marie-Tooth Disease, Type 2C | Osteomalacia | Pigment Dispersion Syndrome | Ocular Hypertension | Withdrawal Syndrome | Idiopathic Multicentric Castleman Disease | Stromal Corneal Dystrophy | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Senior-Loken Syndrome | Cholelithiasis | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Nance-Horan Syndrome | Goiter | Neurofibromatosis Type 2 | Primary Erythromelalgia | Giant Cell Glioblastoma | Odonto-onycho-dermal Dysplasia | T-cell Prolymphocytic Leukemia | Myotonia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Hereditary Hemorrhagic Telangiectasia | Sarcoma | Heart Septal Defects | Pierre Robin Syndrome | Incontinentia Pigmenti | Seizures-scoliosis-macrocephaly Syndrome | Retinoschisis | Smith-Lemli-Opitz Syndrome | Antley-Bixler Syndrome | Familial Digital Arthropathy-brachydactyly | Tibial Muscular Dystrophy | Atelosteogenesis Type 1 | Cri-du-chat Syndrome | Sleep Disorder | Paraplegia | Paraganglioma, Carotid Body | Acrodermatitis Enteropathica | Hypertension, Pulmonary | Acute Motor Axonal Neuropathy | Cushing Syndrome | LRBA Deficiency | Early Infantile Epileptic Encephalopathy 28 | Goiter, Nodular | Necrotizing Autoimmune Myopathy | Cutaneous Lupus Erythematosus | Salla Disease | Osteogenesis Imperfecta | Gerodermia Osteodysplastica | Shock, Cardiogenic | Heterotaxy | Thyroiditis, Autoimmune | IgA Deficiency | Congenital Afibrinogenemia | Myopathy | Spinal Cord Diseases | Isobutyryl-CoA Dehydrogenase Deficiency | Hypertension, Renal | Alagille Syndrome | Osteoporosis | Mixed Connective Tissue Disease | Pure Autonomic Failure | Pancreatitis | Donnai-Barrow Syndrome | Chorea-acanthocytosis | Keratitis | Hypercalciuria | Lathosterolosis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Mountain Sickness | Iron Metabolism Disorders | Fibrosarcoma | Renal Failure | Multiple Epiphyseal Dysplasia | Pontocerebellar Hypoplasia Type 7 | Rett Syndrome | Papilledema | Dermatofibrosarcoma | Borjeson-Forssman-Lehmann Syndrome | Cerebrotendinous Xanthomatosis | Alveolar Capillary Dysplasia | Syndactyly | Dermatitis | Charcot-Marie-Tooth Disease Type 2D | Heterotopic Ossification | Disseminated Intravascular Coagulation | Sitosterolemia | Mast Cell Leukemia | Hyperlipidemia, Familial Combined | Polymyositis | Polycystic Kidney, Autosomal Dominant | Guttate Psoriasis | Retinitis | Neurotoxicity | Hyperbilirubinemia, Neonatal | Spinocerebellar Ataxia Type 31 | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Schnitzler Syndrome | Chronic Neutrophilic Leukemia | Conjunctivitis | Hypertension | WAGR Syndrome | Tendinopathy | Thyroid Hormone Resistance | Nijmegen Breakage Syndrome | Thrombophilia | Lymphomatoid Granulomatosis | Spondyloarthritis | Syphilis | Diabetes Type 2 | Pemphigoid | Mycosis Fungoides | Spina Bifida | Corticobasal Syndrome | Speech Disorders | Alopecia | Aldosterone Synthase Deficiency | Pulmonary Vein Stenosis | Autonomic Nervous System Disorders | Pituitary Dwarfism | Shprintzen-Goldberg Syndrome | Fucosidosis | Gigantism | Martsolf Syndrome | Distal Spinal Muscular Atrophy | Discoid Lupus Erythematosus | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Trichomegaly | Ameloblastic Carcinoma | Congenital Disorders Of Glycosylation | Anorchia | SAPHO Syndrome | Bardet-Biedl Syndrome | Chronic Myeloid Leukemia | Acute Generalized Exanthematous Pustulosis | Infantile Liver Failure Syndrome 1 | Malignant Peripheral Nerve Sheath Tumor | Parkinson Disease 6, Autosomal Recessive Early-onset | Beta-Propeller Protein-associated Neurodegeneration | Nasodigitoacoustic Syndrome | Hypophosphatasia | Wolfram Syndrome 2 | Von Hippel-Lindau Disease | Maple Syrup Urine Disease | Seasonal Mood Disorder | Cancer, Colon | Craniometaphyseal Dysplasia | C3 Glomerulonephritis | Systemic Mastocytosis | Hyperinsulinemic Hypoglycemia | Prader-Willi Syndrome | Anencephaly | Thrombocytopenia | Hepatitis | Arthritis, Reactive | Familial Isolated Hyperparathyroidism | Smoldering Myeloma | Pure Red Cell Aplasia | Gastroenteritis, Eosinophilic | Spinal Muscular Atrophy Type 3 | Loeys-Dietz Syndrome Type 4 | Agnathia-Otocephaly Complex | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Hypertriglyceridemia | Congenital Hereditary Endothelial Dystrophy Type I | Epicondylitis | Methemoglobinemia Type IV | Benign Familial Neonatal Convulsions | Hyperbilirubinemia | Dysfibrinogenemia | Bacterial Meningitis | Adult Polyglucosan Body Disease | Dominant Optic Atrophy | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Disseminated Superficial Actinic Porokeratosis | Methemoglobinemia | Hoyeraal-Hreidarsson Syndrome | Delayed Sleep Phase Syndrome | Osteogenesis Imperfecta Type I | Oligoasthenoteratozoospermia | Spinocerebellar Ataxia Type 27 | B-cell Chronic Lymphocytic Leukemia | Optic Neuropathy, Anterior Ischemic | Hypogonadism | Intermittent Claudication | Aicardi-Goutieres Syndrome | Glomerulonephritis, Membranous | Benign Familial Infantile Seizures | Porokeratosis | Myasthenia Gravis | Blepharitis | Hyperlipidemia | Chondrodysplasia Punctata | Epidermolysis Bullosa Acquisita | Moyamoya Disease | Osteoporosis, Postmenopausal | Primary Lateral Sclerosis | Short-chain Acyl-CoA Dehydrogenase Deficiency | Granular Corneal Dystrophy | Hereditary Elliptocytosis | Facioscapulohumeral Muscular Dystrophy | Woodhouse-Sakati Syndrome | Myoclonus-dystonia Syndrome | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Blue Nevus | Oligospermia | Asthma, Nocturnal | Gaucher Disease | Neutrophilia | Chronic Kidney Disease | Wolcott-Rallison Syndrome | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Hypopituitarism | Congenital Poikiloderma | Methylmalonic Aciduria And Homocystinuria, CblC Type | D-2-Hydroxyglutaric Aciduria | Leiomyosarcoma | Argininosuccinic Aciduria | Jacobsen Syndrome | Chronic Idiopathic Myelofibrosis | Varices | Persistent Hyperplastic Primary Vitreous | Bruck Syndrome | Tonsillitis | Hyperparathyroidism, Secondary | Ameloblastoma | Iron Overload | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Sertoli Cell-only Syndrome | Tinea | Celiac Disease | Facioscapulohumeral Muscular Dystrophy Type 1 | Diabetes | Bone Giant Cell Tumor | Cystitis | Gallstones | Corneal Neovascularization | Cockayne Syndrome | Porphyria, Acute Intermittent | Waardenburg Syndrome Type 2 | Mannosidase Deficiency Diseases | Melanoma, Uveal | Perivascular Epithelioid Cell Tumor | Cirrhosis | Liver Diseases | Macular Degeneration | Asthma, Exercise-induced | Erythropoietic Protoporphyria | Retinitis Pigmentosa | Castleman Disease | Tremor | Tyrosine Hydroxylase Deficiency | Lipid Metabolism Disorders | Renal-hepatic-pancreatic Dysplasia | Axenfeld-Rieger Syndrome | Cornelia De Lange Syndrome | Retinal Diseases | Hyperacusis | Spondyloepiphyseal Dysplasia Tarda, X-linked | Spinocerebellar Ataxia Type 20 | Vitreoretinal Degeneration, Snowflake Type | Peters-plus Syndrome | Neuromyotonia | Intestinal Tuberculosis | Tic Disorder | Familial Mediterranean Fever