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.

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Congenital Bile Acid Synthesis Defect | Retinal Vasculitis | Gray Platelet Syndrome | Osteoglophonic Dysplasia | Lipid Storage Myopathy | CEDNIK Syndrome | GATA2 Deficiency | Cutaneous Angiosarcoma | Pregnancy, Ectopic | Pigment Dispersion Syndrome | Ectrodactyly | Huntington's Disease | Acute Generalized Exanthematous Pustulosis | Varices | Stargardt Disease | Vitelliform Macular Dystrophy | Diffuse Intrinsic Pontine Glioma | Mitochondrial DNA Depletion Syndrome 13 | Corneal Dystrophy And Perceptive Deafness | Neurocysticercosis | Familial Retinal Arterial Macroaneurysm | Erythrokeratodermia Variabilis | Sporadic Hemiplegic Migraine | Rhabdomyosarcoma, Alveolar | Hypertrophy | Bicuspid Aortic Valve | Cardiospondylocarpofacial Syndrome | Cerebellofaciodental Syndrome | Neonatal Progeroid Syndrome | Glycogen Storage Disease Type 0, Muscle | Trichuriasis | Tietze Syndrome | Cancer, Skin | Retinal Coloboma | Synpolydactyly | Pseudohypoparathyroidism Type 1A | Uterine Leiomyoma | Tatton-Brown-Rahman Syndrome | Pre-eclampsia | Eccrine Porocarcinoma | Noonan Syndrome | Peroxisomal Disorder | Long QT Syndrome Type 3 | X-linked Acrogigantism | Sertoli Cell-only Syndrome | Enterocolitis, Necrotizing | Cholestasis, Intrahepatic | Rickets | NDH Syndrome | Prader-Willi Syndrome | Tetraplegia | Joubert Syndrome | Schizencephaly | Nephronophthisis | Juvenile Polyposis | Methemoglobinemia Type IV | Vitamin A Deficiency | Graves Disease | Progressive Familial Intrahepatic Cholestasis Type 2 | Acute Myeloid Leukemia | Avellino Corneal Dystrophy | Polycystic Ovary Syndrome | Diabetes Insipidus, Nephrogenic | Tuberculosis | TARP Syndrome | Amelanotic Melanoma | Cholelithiasis | Dementia, Vascular | Pancytopenia | Chanarin-Dorfman Syndrome | Lennox-Gastaut Syndrome | Tricho-hepato-enteric Syndrome | Spinal Muscular Atrophy Type 2 | Congenital Adrenal Hyperplasia | Meningioma, Benign | X-linked Sideroblastic Anemia | Chondrosarcoma | Pituitary Disorders | Ghosal Syndrome | Isovaleric Acidemia | Hepatorenal Syndrome | Behavioral Variant Of Frontotemporal Dementia | Familial Mediterranean Fever | Pseudohypoaldosteronism | Okihiro Syndrome | Pearson Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Osteopathia Striata With Cranial Sclerosis | Sepiapterin Reductase Deficiency | Duchenne Muscular Dystrophy | Blastomycosis | VACTERL Association | Fibrosarcoma | Charcot-Marie-Tooth Disease Type 4B1 | Stromal Corneal Dystrophy | Hepatitis, Autoimmune | Viral Meningitis | Erectile Dysfunction | Hyperbilirubinemia, Neonatal | Pierpont Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Branchiootorenal Syndrome | Coloboma | Schnitzler Syndrome | Frontotemporal Dementia | Reticular Dysgenesis | Urolithiasis | Takenouchi-Kosaki Syndrome | H Syndrome | Episodic Ataxia Type 1 | Hepatitis B, Chronic | Thrombosis | Borderline Personality Disorder | Agoraphobia | Hemolytic Anemia | Von Willebrand Disease | Cluster Headache | Coronary Heart Disease | Fuchs 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Dyggve-Melchior-Clausen Disease | Colitis, Collagenous | Aromatic L-amino Acid Decarboxylase Deficiency | Pendred Syndrome | Rubeosis Iridis | Chronic Enteropathy Associated With SLCO2A1 Gene | Diabetic Neuropathy | Cellulitis | Cleidocranial Dysplasia | Infantile Spasm | Inborn Errors Of Metabolism | Focal Cortical Dysplasia Type 2 | Gastric Atrophy | Chromosome 5q Deletion Syndrome | Hypoplastic Left Heart Syndrome | Ataxia-ocular Apraxia 2 | Plasmacytoma | Familial Isolated Hyperparathyroidism | Astigmatism | Gastroschisis | Guillain-Barre Syndrome | Acrodysostosis | Cholecystitis | Hypokalemia | Intestinal Pseudo-obstruction | Vitreoretinopathy, Proliferative | Hennekam Lymphangiectasia-lymphedema Syndrome | Polycystic Kidney, Autosomal Recessive | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Basal Cell Nevus Syndrome | Usher Syndrome Type III | Epidermodysplasia Verruciformis | Non-Hodgkin Lymphoma | Congenital Disorders Of Glycosylation | Myhre Syndrome | Congenital 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