Encephalomyopathic Form Mitochondrial DNA Depletion Syndrome
Encephalomyopathic Form Mitochondrial DNA Depletion Syndrome
About the Disease
Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, also known as mtdna depletion syndrome, encephalomyopathic form, is related to mitochondrial dna depletion syndrome 5 and mitochondrial dna depletion syndrome 8a.
Common Targets
ACAD9 | FBXL4 | TWNK | SUCLG1 | TK2 | SUCLA2 | TYMP
Note: If you'd like to get a target analysis report for Encephalomyopathic Form Mitochondrial DNA Depletion Syndrome, 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 Encephalomyopathic Form Mitochondrial DNA Depletion Syndrome at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.
Other Diseases
Pemphigus Vulgaris | Craniolenticulosutural Dysplasia | Williams Syndrome | Kearns-Sayre Syndrome | N-acetylglutamate Synthase Deficiency | Gray Platelet Syndrome | Focal Segmental Glomerulosclerosis | Lattice Corneal Dystrophy Type 1 | Porphyria, Variegate | Enterocolitis, Necrotizing | Lung Diseases | Myoclonic Atonic Epilepsy | Homocystinuria | Tetanus | Cryptosporidiosis | Rotor Syndrome | Macrophagic Myofasciitis | Urofacial Syndrome | SAPHO Syndrome | Distal Spinal Muscular Atrophy | Thalassemia, Beta | Hydrops Fetalis | Heterotopic Ossification | Perry Syndrome | Meningeal Melanocytoma | Angiosarcoma | Common Variable Immunodeficiency | Becker Muscular Dystrophy | Anencephaly | Thin Basement Membrane Disease | Spondyloepiphyseal Dysplasia Tarda, X-linked | Paget's Disease Of The Breast | Hydrocephalus, Normal Pressure | Eosinophilia | Postaxial Polydactyly | Non-Langerhans Cell Histiocytosis | Fabry's Disease | Pure Red Cell Aplasia | Spinocerebellar Ataxia Type 14 | Platelet Disorders | Pleural Tuberculosis | Fatty Aldehyde Dehydrogenase Deficiency | Stroke, Ischemic | Schaaf-Yang Syndrome | Neurofibrosarcoma | Schwartz-Jampel-Aberfeld Syndrome | Alexander Disease | Postpartum Depression | Rubeosis Iridis | Jawad Syndrome | Babesiosis | Blepharitis | Hyperglycemia | Opisthorchiasis | Hypopigmentation | Rheumatic Heart Disease | Venous Insufficiency | Acrocallosal Syndrome | Oculocutaneous Albinism Type 1 | Hemangioblastoma | Nance-Horan Syndrome | Epidermolytic Palmoplantar Keratoderma | Chorea | Familial Hypertrophic Cardiomyopathy | Pheochromocytoma | Craniofrontonasal Syndrome | Retinal Dystrophy | Carbonic Anhydrase VA Deficiency | Neurofibromatosis | Oguchi Disease-2 | Low Phospholipid Associated Cholelithiasis | Fanconi Syndrome | HELLP Syndrome | High Molecular Weight Kininogen Deficiency | Abetalipoproteinemia | Cantu Syndrome | Preaxial Polydactyly | Oculocutaneous Albinism Type 2 | Glycogen Storage Disease Type 9 | Enlarged Vestibular Aqueduct | Knobloch Syndrome | D-2-Hydroxyglutaric Aciduria | Spina Bifida | Cholelithiasis | Aromatic L-amino Acid Decarboxylase Deficiency | Prurigo Nodularis | Myopia | Cholecystitis | Tonsillitis | Craniometaphyseal Dysplasia | Sialidosis | Adenoma, Pituitary | Psoriasis | Glomerulonephritis, Membranoproliferative | Cholera | Dengue Hemorrhagic Fever | Hepatitis, Alcoholic | Cole-Carpenter Syndrome | Microcephalic Primordial Dwarfism | Cleidocranial Dysplasia | Hereditary Mixed Polyposis Syndrome | Mood Disorder | Cancer, Colon | Wolcott-Rallison Syndrome | Fundus Albipunctatus | Hereditary Neuropathy With Liability To Pressure Palsies | Anti-glomerular Basement Membrane Disease | Purpura, Thrombotic Thrombocytopenic | Chondrosarcoma | Eosinophilic Asthma | Chorioretinitis | Osteoporosis-pseudoglioma Syndrome | Congenital Dysfibrinogenemia | Bicuspid Aortic Valve | Dermatomyositis | Sarcoidosis, Pulmonary | Branchiootorenal Syndrome | Persistent Fetal Circulation | Usher Syndrome Type IIC | Astigmatism | Lipid Storage Diseases | Heroin Dependence | Alagille Syndrome | Klippel-Feil Syndrome | Diffuse Palmoplantar Keratoderma | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | VACTERL Association | Plasma Cell Dyscrasia | Skin Papilloma | Primary Pigmented Nodular Adrenocortical Disease | Epicondylitis | C3 Glomerulonephritis | Gliosarcoma | Mandibuloacral Dysplasia With Type A Lipodystrophy | Hypoplastic Left Heart Syndrome | Pseudohypoparathyroidism Type 1A | Non-bullous Congenital Ichthyosiform Erythroderma | Osteonecrosis | Toxic Epidermal Necrolysis | Cryptococcal Meningitis | Disseminated Intravascular Coagulation | Cousin Syndrome | Evans Syndrome | Neovascular Glaucoma | Sleep Apnea | Borderline Personality Disorder | Constipation | Hypertension, Renal | Lichen Sclerosus | LMNA-related Congenital Muscular Dystrophy | Retinal Degeneration | Sandhoff Disease | 3-methylglutaconic Aciduria Type I | Retinopathy Of Prematurity | Pigment Dispersion Syndrome | Charcot-Marie-Tooth Disease Type 2D | Herpes Simplex Dermatitis | Congenital Stromal Corneal Dystrophy | Bone Marrow Necrosis | Temporal Lobe Epilepsy | Learning Disability | Cholestasis, Intrahepatic | Optic Nerve Diseases | Ocular Albinism Type 1 | Sleep Apnea, Central | Prader-Willi Syndrome | Kabuki Syndrome | Seborrheic Dermatitis | Chylomicron Retention Disease | Hypertensive Retinopathy | Beckwith-Wiedemann Syndrome | Epilepsy, Generalized | Danon Disease | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Keratosis | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Porokeratosis | Spinal Cord Diseases | Hepatitis A | Mucormycosis | Left Ventricular Noncompaction | Neuroma | Meningioma, Benign | Mastitis | Autoimmune Disease | Schindler Disease | Cancer, Kidney | Limb Girdle Muscular Dystrophy | Microcephaly | Uveitis, Anterior | Neuroendocrine Cancer | Pituitary Dwarfism | Auriculocondylar Syndrome | Larsen Syndrome | Retinitis | Osteoglophonic Dysplasia | Alazami Syndrome | Pantothenate Kinase-associated Neurodegeneration | Cabezas Syndrome | Malignant Fibrous Histiocytoma | Sturge-Weber Syndrome | Discoid Lupus Erythematosus | Varicocele | Cyst | Spinocerebellar Ataxia Type 13 | Combined Malonic And Methylmalonic Acidemia | Raynaud Phenomenon | Melanoma, Uveal | Nephrosclerosis | Schizotypal Personality Disorder | Thrombotic Microangiopathy | Vitamin D Deficiency | Heavy Chain Disease | Hemolytic Uremic Syndrome | Oculopharyngeal Muscular Dystrophy | Down Syndrome | Leukocyte Adhesion Deficiency | Hemochromatosis | Situs Inversus | Angioedema | Li-Fraumeni Syndrome | Camurati-Engelmann Disease | Marinesco-Sjogren Syndrome | Aphasia | Congenital Torticollis | Pseudoachondroplasia | Azoospermia | Hyperacusis | Peutz-Jeghers Syndrome | Metatropic Dysplasia | Sarcoidosis | Mosaic Variegated Aneuploidy Syndrome 2 | Hamartoma | Charcot-Marie-Tooth Disease Type 3 | Tyrosine Hydroxylase Deficiency | Waardenburg Syndrome | Migraine | Smoldering Myeloma | Episodic Ataxia | Rosacea | Premenstrual Syndrome | Cri-du-chat Syndrome | Congenital Lipoid Adrenal Hyperplasia | Primary Lateral Sclerosis | Sengers Syndrome | Prostatitis | Vitelliform Macular Dystrophy | Spinocerebellar Ataxia Type 42 | Autosomal Recessive Spastic Paraplegia Type 75 | Mannosidase Deficiency Diseases | Tyrosinemia Type 1 | Hyperlipidemia Type V | Neurotoxicity | Carotid Artery Disease | Hereditary Pyropoikilocytosis | Microphthalmia | Hypercholesterolemia | Hepatopulmonary Syndrome | Lymphangiomatosis | Ligneous Conjunctivitis | Stargardt Disease | Wilson's Disease | Esophageal Adenocarcinoma | Best Macular Dystrophy | Mevalonate Kinase Deficiency | Hypermetropia | Episodic Ataxia Type 2 | Atrial Septal Defect | VACTERL/VATER Association | Chiari Malformation Type I | Hyperparathyroidism-jaw Tumor Syndrome | Aldosteronism | CREST Syndrome | Osteomalacia | Multiple Sclerosis, Secondary Progressive | Myoclonus-dystonia Syndrome | Spinocerebellar Ataxia Type 3 | Inflammatory Bowel Disease | Prolactinoma | Glutaric Aciduria Type 1 | Basan Syndrome | Hypophosphatasia | MELAS Syndrome | Spinal Muscular Atrophy Type 2 | Intracranial Hypertension | Anxiety Disorders | Hypercholesterolemia, Familial | Cardiomyopathy, Hypertrophic | Juvenile Xanthogranuloma | Meningioma | Small Lymphocytic Lymphoma | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Blue Rubber Bleb Nevus Syndrome | Spinocerebellar Ataxia Type 20 | Gout | Chanarin-Dorfman Syndrome | Mast Cell Leukemia | Meier-Gorlin Syndrome | Heart Block | Seizures-scoliosis-macrocephaly Syndrome | Mitochondrial Encephalomyopathy | Mitochondrial Disease | Hypotrichosis | Overactive Bladder | Hereditary Xerocytosis | Nephropathy | Specific Granule Deficiency | Prediabetes | Neuromyelitis Optica | Osteosarcoma | Dermatitis Herpetiformis | Epithelial-myoepithelial Carcinoma | Papillorenal Syndrome | Richter's Syndrome | Synovitis | Arthritis, Psoriatic | Dyslipidemia | Tetraplegia | Leprosy | Ectodermal Dysplasia | Fibromyalgia | Pilomatrix Carcinoma | Stromal Corneal Dystrophy | Angina Pectoris | Polyradiculopathy | Muscle Wasting | Iron Metabolism Disorders | Deafness, Dystonia, And Cerebral Hypomyelination | HANAC Syndrome | Pseudohypoparathyroidism Type 1B | Dystonia-parkinsonism, X-linked | Orotic Aciduria | Tangier Disease | Myelofibrosis | Amish Infantile Epilepsy Syndrome | Glanzmann Thrombasthenia | Progressive Encephalopathy-optic Atrophy Syndrome | Metabolic Syndrome | Hypodontia | Phosphoglycerate Dehydrogenase Deficiency | Heterotaxy | Autoimmune Polyendocrinopathy Syndrome Type I | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Congenital Dyserythropoietic Anemia Type 4 | Schnyder Crystalline Corneal Dystrophy | Communication Disorders | Enhanced S-cone Syndrome | Long QT Syndrome Type 3 | Pain | Sickle Cell Disease | Transcobalamin Deficiency | Carpal Tunnel Syndrome | Traboulsi Syndrome | Combined Pituitary Hormone Deficiency | Familial Hyperaldosteronism | Myelitis | Japanese Encephalitis | Hypercalciuria | Autoimmune Hemolytic Anemia | Triphalangeal Thumb-polysyndactyly Syndrome | Arthritis | Protein C Deficiency | Neuromyotonia | Chronic Mucocutaneous Candidiasis | Schistosomiasis Mansoni | Lipid Storage Myopathy | Thromboembolism | Diabetes Insipidus | Acquired Partial Lipodystrophy | Dowling-Degos Disease | Glioblastoma | Intermittent Claudication | Asplenia | Gallstones | Encephalitis, Tick-borne | Lymphangioleiomyomatosis | Sarcoma, Ewing | Restless Legs Syndrome | Ameloblastic Carcinoma | Muir-Torre Syndrome | Maternally Inherited Diabetes And Deafness | Occipital Neuralgia | Thrombocytopenia | Autism Spectrum Disorders | Myositis | Panniculitis | Renal-hepatic-pancreatic Dysplasia | Keratocystic Odontogenic Tumor | Hemochromatosis Type 2 | Pseudohypoparathyroidism Type 2 | Focal Dermal Hypoplasia | Leukodystrophies | Desmosterolosis | Astrocytoma, Anaplastic | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Sleep Apnea, Obstructive | Lamellar Ichthyosis | Cholestasis | IgA Nephropathy | Myopathy