Maternally Inherited Diabetes And Deafness

About the Disease
Diabetes and Deafness, Maternally Inherited, also known as midd, is related to mitochondrial myopathy and mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. An important gene associated with Diabetes and Deafness, Maternally Inherited is MT-TE (Mitochondrially Encoded TRNA-Glu (GAA/G)). The drugs 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid and Protective Agents have been mentioned in the context of this disorder. Affiliated tissues include eye, retina and heart, and related phenotypes are constipation and type ii diabetes mellitus

Common Targets
RNR1 | COX3 | CFD | CYTB | ND3 | TRNA | ARMS2 | Complement Complex | ND4 | ATP6 | CFH | ND4L | ND5 | TRNL1 | COX1 | ND6 | COX2

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

Other Diseases

Systemic Mastocytosis | Marinesco-Sjogren Syndrome | Aspergillosis | Learning Disability | C3 Glomerulopathy | Cervical Dystonia | B-cell Prolymphocytic Leukemia | Vitreoretinal Degeneration, Snowflake Type | Chiari Malformation Type I | Hereditary Coproporphyria | Thymoma, Malignant | Hemophilia | Glycogen Storage Disease Type 1a | Uterine Leiomyoma | Sporadic Hemiplegic Migraine | Alpha-thalassemia Myelodysplasia Syndrome | Thrombocytopenia | Optic Neuropathy | Cholestasis | Spinocerebellar Ataxia Type 17 | Congenital Nephrotic Syndrome | Anodontia | Hereditary Mixed Polyposis Syndrome | Polymicrogyria | Herpes Genitalis | LEOPARD Syndrome | Focal Segmental Glomerulosclerosis | Diabetes Mellitus, Transient Neonatal | Xeroderma Pigmentosum | Congenital Bilateral Absence Of Vas Deferens | Autonomic Neuropathy | Charcot-Marie-Tooth Disease Type 2T | Myoclonus-dystonia Syndrome | Epidermodysplasia Verruciformis | Myelitis, Transverse | Neurogenic Bladder | Porphyria, Acute Intermittent | Chondrosarcoma | Parapsoriasis | Auriculocondylar Syndrome | IgA Deficiency | Focal Cortical Dysplasia Type 2 | Pericarditis | Sleep Apnea | Neurofibromatosis-Noonan Syndrome | Combined Deficiency Of Factor V And Factor VIII | Tatton-Brown-Rahman Syndrome | Mood Disorder | Prostatitis | Posterior Polar Cataract | Sickle Cell Disease | Best Macular Dystrophy | Uveitis | Anti-NMDA Receptor Encephalitis | Tricho-hepato-enteric Syndrome | Albinism | Arthritis, Gouty | Burn-McKeown Syndrome | Chitayat Syndrome | Autoimmune Polyendocrine Syndrome | Small Lymphocytic Lymphoma | ADNP Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | GAPO Syndrome | Bursitis | Kindler Syndrome | Hereditary Pyropoikilocytosis | Crigler-Najjar Syndrome | Tic Disorder | Dysferlinopathy | Cyst | Toxoplasmosis | Glycogen Storage Disease Type 0, Muscle | Coronary Heart Disease | Canavan Disease | Synpolydactyly | Dupuytren Disease | Ependymoma | Riboflavin Transporter Deficiency Neuronopathy | Corticobasal Syndrome | Neovascular Glaucoma | Meleda Disease | Gray Platelet Syndrome | Bardet-Biedl Syndrome | Benign Hereditary Chorea | Holt-Oram Syndrome | Bare Lymphocyte Syndrome | CREST Syndrome | Leber Hereditary Optic Neuropathy | Mumps | Thalassemia, Beta | Neonatal Progeroid Syndrome | Dermatitis Herpetiformis | Charcot-Marie-Tooth Disease | Axenfeld-Rieger Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Anuria | Cantu Syndrome | Succinic Semialdehyde Dehydrogenase Deficiency | Sleep Apnea, Obstructive | Stickler Syndrome | Meckel-Gruber Syndrome | DRESS Syndrome | Pseudoexfoliation Syndrome | Renal Hypouricemia | Myositis | Herpes Simplex Dermatitis | Papilledema | Spinocerebellar Ataxia Type 2 | Bronchiectasis | Spasticity | Vestibular Disease | Cryopyrin-associated Periodic Syndromes | Low Phospholipid Associated Cholelithiasis | Keratoconjunctivitis | Arthritis | Seizures | Chromosome 5q Deletion Syndrome | Usher Syndrome Type III | Esotropia | Pulmonary Stenosis | Renal-hepatic-pancreatic Dysplasia | Episodic Ataxia | Pontocerebellar Hypoplasia | Diamond-Blackfan Anemia | Intracerebral Hemorrhage | Lathosterolosis | MIRAGE Syndrome | Diabetic Macular Edema | Panic Disorder | Sepiapterin Reductase Deficiency | N-acetylglutamate Synthase Deficiency | Facioscapulohumeral Muscular Dystrophy Type 2 | Chondromyxoid Fibroma | Hyperacusis | Thrombophilia | Familial Advanced Sleep Phase Syndrome | Hyperthyroidism | Pontocerebellar Hypoplasia Type 7 | Pycnodysostosis | Adult Polyglucosan Body Disease | WAGR Syndrome | Cardiac Sarcoidosis | Osteogenesis Imperfecta Type VI | Wolman Disease | Neuromuscular Disorders | Liddle Syndrome | Milk Allergy | Cancer, Prostate | Neuroendocrine Cancer | Skin Fragility-woolly Hair Syndrome | Tyrosine Hydroxylase Deficiency | Hyperlipidemia | Amelanotic Melanoma | Thyroid Dysgenesis | Rubeosis Iridis | Mucormycosis | Transient Bullous Dermolysis Of The Newborn | Nance-Horan Syndrome | Lymphoproliferative Disorders | Schizophrenia | Erysipelas | Adenylosuccinate Lyase Deficiency | Poirier-Bienvenu Neurodevelopmental Syndrome | Optic Neuritis | Bronchitis, Chronic | Myasthenia Gravis | Infantile Nephropathic Cystinosis | Neurofibromatosis Type 1 | Purpura, Thrombotic Thrombocytopenic | Niemann-Pick Disease, Type B | Isobutyryl-CoA Dehydrogenase Deficiency | Hyperuricemic Nephropathy, Familial Juvenile | Erythematotelangiectatic Rosacea | Carey-Fineman-Ziter Syndrome | Diarrhea | Saul-Wilson Syndrome | HELLP Syndrome | Arts Syndrome | Gastroschisis | Castleman Disease | Rhinitis | Enhanced S-cone Syndrome | Blepharophimosis Syndrome | Multiple Sulfatase Deficiency | Medulloblastoma | Leukocyte Adhesion Deficiency | Lipid Storage Myopathy | Thalassemia | Lipid Metabolism Disorders | Distal Spinal Muscular Atrophy | Benign Familial Infantile Seizures | Absence Epilepsy | Macrophage Activation Syndrome | Agranulocytosis | Meconium Ileus | Pulmonary Capillary Hemangiomatosis | Primary Torsion Dystonia | Pemphigoid | Tumoral Calcinosis | Cleidocranial Dysplasia | Urofacial Syndrome | Kleine-Levin Syndrome | Coronary Artery Disease | Dystrophy, Cone-rod | Varices | Prolymphocytic Leukemia | Pyloric Stenosis, Infantile Hypertrophic | Glanzmann Thrombasthenia | Non-bullous Congenital Ichthyosiform Erythroderma | Angina Pectoris | Early Infantile Epileptic Encephalopathy | 3-methylcrotonyl-CoA Carboxylase Deficiency | Spinocerebellar Ataxia Type 13 | Avellino Corneal Dystrophy | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Lissencephaly 2 | 3-M Syndrome | Dystonia Musculorum Deformans | Perivascular Epithelioid Cell Tumor | Urticaria | Porokeratosis | Pseudomyxoma Peritonei | Hypervalinemia | Hereditary Spherocytosis | Glycogen Storage Disease Type 3 | Fucosidosis | Meningococcal Infections | Hydrolethalus Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Lymphoma, Mantle Cell | Hypertension, Portal | Glaucoma | Nephrotic Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Primary Hyperoxaluria Type 3 | 3-hydroxy-3-methylglutaric Aciduria | Hypotrichosis | Ataxia-ocular Apraxia 2 | Glomerulonephritis, Membranous | Clouston Hidrotic Ectodermal Dysplasia | Hyperhomocysteinemia | Cellulitis | Pineoblastoma | Retinopathy Of Prematurity | Hereditary Neuropathy With Liability To Pressure Palsies | Beta-Propeller Protein-associated Neurodegeneration | Meningeal Melanocytoma | Brooke-Spiegler Syndrome | Alopecia Areata | Venous Insufficiency | IgA Nephropathy | Retinal Degeneration | Hepatitis C, Chronic | Duchenne Muscular Dystrophy | Mandibuloacral Dysplasia With Type A Lipodystrophy | Renpenning Syndrome | Sjogren Syndrome | Mucolipidosis Type IV | Polycythemia Vera | Glutaric Aciduria Type 1 | Atopic Dermatitis | Pyelonephritis | Panniculitis | Pilomatrix Carcinoma | Seminoma | Pneumonia, Bacterial | Huntington's Disease | Necrobiosis Lipoidica | Adenoma, Villous | Hyperandrogenemia | Congenital Bile Acid Synthesis Defect | Encephalopathy, Glycine | Angelman Syndrome | Leukoplakia, Oral | Gastroenteritis, Eosinophilic | Glioblastoma | Lymphomatoid Granulomatosis | Goldenhar Syndrome | Acanthosis Nigricans | Ocular Albinism Type 1 | Corneal Dystrophies, Hereditary | Hyperlipidemia Type V | Congenital Tufting Enteropathy | Lymphangioleiomyomatosis | Pouchitis | Malnutrition | Poretti-Boltshauser Syndrome | Colitis | Bronchitis | Prune Belly Syndrome | Krabbe Disease | Hypereosinophilic Syndrome | AIDS | Poikiloderma With Neutropenia | PASLI Disease | Retinal Vasculitis | Cutaneous Lupus Erythematosus | Skin Carcinoma | Cerebellofaciodental Syndrome | Acute Kidney Injury | Major Depression | Spinal Muscular Atrophy | Down Syndrome | Coffin-Lowry Syndrome | Focal Facial Dermal Dysplasia | Aplasia Cutis Congenita | Inborn Errors Of Metabolism | Veno-occlusive Disease | Osteoarthritis | Ureteropelvic Junction Obstruction | Chloridorrhea, Congenital | Ovarian Hyperstimulation Syndrome | Cushing Syndrome | Vulvovaginitis | Spina Bifida | Parkinson Disease 6, Autosomal Recessive Early-onset | Immunoproliferative Disorders | Hyperkalemic Periodic Paralysis | Hyperlipidemia, Familial Combined | Acute Lymphocytic Leukemia | Retinoschisis | Congenital Muscular Dystrophy | Gnathodiaphyseal Dysplasia | Epidermal Nevus Syndrome | Agammaglobulinemia | Myoclonus | Retinoblastoma | Epidermolytic Hyperkeratosis | Mevalonate Kinase Deficiency | Familial Dysautonomia | Malonyl-CoA Decarboxylase Deficiency | Aarskog-Scott Syndrome | Spondylocarpotarsal Synostosis Syndrome | Mastitis | Hepatitis B, Chronic | Dementia, Vascular | VACTERL Association | Early Infantile Epileptic Encephalopathy 1 | Kearns-Sayre Syndrome | Neurofibrosarcoma | Prurigo Nodularis | Diabetes Insipidus, Neurogenic | Insulin Resistance | Primary Ovarian Insufficiency | Protein C Deficiency | McLeod Syndrome | Branchiootorenal Syndrome | Hypophosphatasia | Primary Cutaneous Amyloidosis | Retinal Dystrophy, Early-onset Severe | Portal Vein Thrombosis | Campomelic Dysplasia | Open-angle Glaucoma | Spinocerebellar Ataxia Type 40 | Goiter, Nodular | Exostoses | Chronic Periodontitis | Hypertelorism | Sandhoff Disease | Infantile Spasm | Brugada Syndrome 1 | Early Infantile Epileptic Encephalopathy 13 | Dowling-Degos Disease | Methylmalonic Aciduria And Homocystinuria, CblC Type | Hemorrhage | Conjunctivitis | Lentigo | Ganglioneuroma | Leukoplakia | Acute Anterior Uveitis | Episodic Ataxia Type 1 | Renal Oncocytoma | SAPHO Syndrome | Miyoshi Myopathy | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Pulmonary Sclerosing Hemangioma | Sick Sinus Syndrome 1 | Syndactyly | Acquired Partial Lipodystrophy | DOCK8 Immunodeficiency Syndrome | Microvillus Inclusion Disease | Leukoencephalopathy, Progressive Multifocal | Keratitis-ichthyosis-deafness Syndrome | Carbohydrate Metabolism Disorders | Hyperekplexia | Cholelithiasis | Spinocerebellar Ataxia Type 14 | Polycystic Ovary Syndrome | Lipid Storage Diseases | Optic Nerve Hypoplasia, Bilateral | Ameloblastic Carcinoma | Pneumococcal Meningitis | Silicosis | Wolfram Syndrome 2 | C3 Glomerulonephritis | Otitis Media | Ehlers-Danlos Syndrome | Glomerulonephritis