Disease

Nemaline Myopathy 8

About the Disease
Nemaline Myopathy 8, also known as nemaline myopathy 8, autosomal recessive, is related to nemaline myopathy and respiratory failure. An important gene associated with Nemaline Myopathy 8 is KLHL40 (Kelch Like Family Member 40), and among its related pathways/superpathways is Striated muscle contraction pathway. Affiliated tissues include skeletal muscle, and related phenotypes are dysphagia and facial palsy

Common Targets
KLHL40

疾病靶点研报
Nemaline Myopathy 8

Note: If you'd like to get a target analysis report for Nemaline Myopathy 8, 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 Nemaline Myopathy 8 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Low Tension Glaucoma | Leber Hereditary Optic Neuropathy | Cerebral Cavernous Malformations | Diabetes Mellitus, Transient Neonatal | Hydrocephalus | Bartter Syndrome | Dementia | Smith-Magenis Syndrome | Pelvic Inflammatory Disease | Alzheimer Disease, Late Onset | Nasodigitoacoustic Syndrome | Distal Spinal Muscular Atrophy | Dystonia Musculorum Deformans | Methemoglobinemia | Phenylketonuria II | Erdheim-Chester Disease | Pyruvate Kinase Deficiency | Parapsoriasis | Meningioma | Congenital Afibrinogenemia | Papilloma | Primrose Syndrome | Carbohydrate Metabolism Disorders | Restrictive Dermopathy | GM2-gangliosidosis AB Variant | Light Chain Amyloidosis | Stomatitis | Chronic Myeloid Leukemia | Coronary Artery Disease | Ollier Disease | Subacute Sclerosing Panencephalitis | Multiple Sclerosis, Primary Progressive | Congenital Ichthyosiform Erythroderma | ADNP Syndrome | Lewy Body Dementia | Lissencephaly 2 | Marfan Syndrome | Creatine Deficiency Syndrome | Hypoplastic Left Heart Syndrome | Charcot-Marie-Tooth Disease Type 3 | Polymyositis | Sialoadenitis | Intestinal Hypomagnesemia 1 | Poretti-Boltshauser Syndrome | Hartsfield Syndrome | Cat Eye Syndrome | Patent Foramen Ovale | Reticular Dysgenesis | Fraser Syndrome | Anorectal Fistula | POEMS Syndrome | Chitayat Syndrome | Saul-Wilson Syndrome | Stickler Syndrome | Lyme Disease | Personality Disorders | Gaucher Disease | Emery-Dreifuss Muscular Dystrophy | Juvenile Polyposis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Pemphigus | Vitamin B12 Deficiency | Esophagitis, Eosinophilic | Primary Hyperoxaluria | Fascioliasis | Arthritis, Psoriatic | Polyarteritis Nodosa | Pemphigus Vulgaris | Overactive Bladder | Pemphigoid | Fibromyalgia | Meningitis | Heart Septal Defects | Vitreoretinopathy, Proliferative | Osmotic Demyelination Syndrome | Central Pain Syndrome | Irritable Bowel Syndrome | Congenital Heart Defects | Carpal Tunnel Syndrome | Wolff-Parkinson-White Syndrome | Intermittent Claudication | Wolman Disease | Metaphyseal Chondrodysplasia, Schmid Type | Spinocerebellar Ataxia Type 42 | Toxoplasmosis | Dermatitis | Non-Langerhans Cell Histiocytosis | Mast Cell Leukemia | Meleda Disease | Progressive Familial Intrahepatic Cholestasis Type 2 | Congenital Poikiloderma | Cornelia De Lange Syndrome | Porphyria, Variegate | Budd-Chiari Syndrome | Hypospadias | Renal Hypouricemia | Lymphoma, Mantle Cell | Hypothalamic Obesity | Varices | Palmoplantar Keratoderma | Episodic Ataxia Type 2 | Pseudo-pseudohypoparathyroidism | Giant Cell Arteritis | Pseudomyxoma Peritonei | Diabetes Insipidus, Neurogenic | Galloway-Mowat Syndrome | D-2-Hydroxyglutaric Aciduria | Leukoencephalopathy, Progressive Multifocal | Polycystic Ovary Syndrome | Hereditary Elliptocytosis | Glomerulonephritis, Membranous | Cysticercosis | Carey-Fineman-Ziter Syndrome | Cancer, Skin | Esthesioneuroblastoma | Nephroblastoma | Schizophrenia, Paranoid | Primary Lateral Sclerosis | Ureteropelvic Junction Obstruction | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Alcoholism | Connective Tissue Disorders | Sick Sinus Syndrome | Cataplexy | Melanoma | Ventricular Septal Defect | Distal Myopathy | Small Lymphocytic Lymphoma | Anosmia, Congenital | Sleep Apnea, Central | Diabetes Gestational | X-linked Charcot-Marie-Tooth Disease | Glycogen Storage Disease Type 1b | Thrombotic Microangiopathy | Lactose Intolerance | Monilethrix | Dysthymia | Niemann-Pick Disease, Type B | Smoldering Myeloma | Alstrom Syndrome | Rett Syndrome | Autoimmune Autonomic Ganglionopathy | Congenital Diaphragmatic Hernia | Spondyloepiphyseal Dysplasia Tarda, X-linked | Peyronie's Disease | Alpers Syndrome | Craniopharyngioma | B-cell Prolymphocytic Leukemia | Sturge-Weber Syndrome | Cannabis Abuse | Glanzmann Thrombasthenia | Zellweger Syndrome | Osteogenesis Imperfecta Type I | Marshall-Smith Syndrome | Angioimmunoblastic T-cell Lymphoma | Erythropoietic Protoporphyria | Fowler's Syndrome | Johanson-Blizzard Syndrome | Stromal Corneal Dystrophy | Spinocerebellar Ataxia Type 7 | Chondrosarcoma | Constipation | Retinal Dystrophy, Early-onset Severe | Azoospermia | Spinal Muscular Atrophy | Isobutyryl-CoA Dehydrogenase Deficiency | Lymphoproliferative Disorders | Myopathy | Transthyretin-related Amyloidosis | Diffuse Intrinsic Pontine Glioma | Pulmonary Vein Stenosis | Hypertriglyceridemia | Congenital Disorders Of Glycosylation | Neuroectodermal Tumors, Primitive | Microcephaly | Adenoma, Pituitary | Spondyloperipheral Dysplasia | Cirrhosis | Macular Corneal Dystrophy Type 1 | Myopia | Bainbridge-Ropers Syndrome | Macular Degeneration | Williams Syndrome | Bronchiectasis | Retinal Vasculitis | Early Infantile Epileptic Encephalopathy 1 | Focal Dermal Hypoplasia | Pancreatitis, Chronic | Cystinuria | Pure Autonomic Failure | Tyrosinemia Type 2 | Kernicterus | Crohn's Disease | Mitochondrial DNA Depletion Syndrome | Osteogenesis Imperfecta Type V | Spondyloarthritis | Open-angle Glaucoma | Pigment Dispersion Syndrome | Trismus-pseudocamptodactyly Syndrome | Myositis | X-linked Myotubular Myopathy | Charcot-Marie-Tooth Disease Type 4D | Partington Syndrome | Epidermolytic Palmoplantar Keratoderma | Osteogenesis Imperfecta Type III | Vitamin A Deficiency | Pierpont Syndrome | Crimean-Congo Hemorrhagic Fever | Hemophagocytic Lymphohistiocytosis | Netherton Syndrome | Majeed Syndrome | Dupuytren Disease | Pyelonephritis | Spinocerebellar Ataxia Type 20 | Acrodermatitis | Gastroenteritis, Eosinophilic | Torticollis | Congenital Lipoid Adrenal Hyperplasia | Mevalonate Kinase Deficiency | Liddle Syndrome | Ectodermal Dysplasia | Pregnancy, Ectopic | Spinocerebellar Ataxia Type 5 | Panniculitis | Spondylocarpotarsal Synostosis Syndrome | Hyperglycemia | Chronic Myelomonocytic Leukemia | NGLY1 Deficiency | Glucagonoma | Hypermetropia | Adenocarcinoma | Plasma Cell Dyscrasia | Miyoshi Myopathy | Moyamoya Disease | Still Disease | Encephalitis, Tick-borne | Lathosterolosis | Hypercalcemia | Nemaline Myopathy | Lymphoma Lymphoblastic | Neonatal Progeroid Syndrome | Cri-du-chat Syndrome | Peritonitis | Dyslipidemia | Dystonia | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Pulmonary Tuberculosis | Diabetes Insipidus, Nephrogenic | Hepatoblastoma | Purpura, Thrombotic Thrombocytopenic | Congenital Central Hypoventilation Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Migraine | Multiple System Atrophy | Ectopia Lentis, Isolated, Autosomal Recessive | Triple A Syndrome | Congenital Adrenal Hyperplasia | Synpolydactyly | Esophageal Carcinoma | Hypersensitivity Pneumonitis | Rhizomelic Chondrodysplasia Punctata | Anencephaly | Dowling-Degos Disease | Bare Lymphocyte Syndrome | Hemorrhagic Disorders | Hepatitis E | Arthrogryposis | Werner's Syndrome | Language Disorders | Epilepsy Of Infancy With Migrating Focal Seizures | 3-M Syndrome | Vitamin K Deficiency | Vici Syndrome | Low Phospholipid Associated Cholelithiasis | Liver Failure | Behcet's Disease | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Aspergillosis | Spinocerebellar Ataxia Type 8 | Hypercholesterolemia | Crisponi Syndrome | Optic Neuropathy, Anterior Ischemic | Fatty Aldehyde Dehydrogenase Deficiency | Erythematotelangiectatic Rosacea | Sarcomatoid Carcinoma Of The Lung | Pneumonia, Mycoplasma | Pneumonia, Viral | Fukuyama Congenital Muscular Dystrophy | Oligoastrocytoma | Hemolytic Uremic Syndrome | Primary Progressive Aphasia | Conn Syndrome | Infantile Liver Failure Syndrome 1 | Mixed Connective Tissue Disease | Peeling Skin Syndrome Type B | Lesch-Nyhan Syndrome | Diffuse Mesangial Sclerosis | Retinal Degeneration | Cystinosis | Giant Cell Glioblastoma | Schuurs-Hoeijmakers Syndrome | Sezary Syndrome | Sleep Apnea | Gastric Atrophy | Benign Familial Infantile Seizures | Scapuloperoneal Spinal Muscular Atrophy | Agranulocytosis | Choriocarcinoma | Temporal Lobe Epilepsy | Methemoglobinemia Type IV | Leishmaniasis, Cutaneous | Lipid Metabolism Disorders | Waardenburg Syndrome Type 2E | Alveolar Capillary Dysplasia | 3-methylglutaconic Aciduria Type IV | Guanidinoacetate Methyltransferase Deficiency | Localized Scleroderma | Pancreatitis | Diffuse Palmoplantar Keratoderma | Rheumatoid Arthritis | Erectile Dysfunction | Malignant Peripheral Nerve Sheath Tumor | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Spinocerebellar Ataxia Type 3 | Spina Bifida | Asthma | Pheochromocytoma | Amblyopia | GATA2 Deficiency | Roberts Syndrome | Coffin-Lowry Syndrome | Ectrodactyly | Bernard-Soulier Syndrome | Sponastrime Dysplasia | Papulopustular Rosacea | Mohr-Tranebjaerg Syndrome | Anti-glomerular Basement Membrane Disease | Nicolaides-Baraitser Syndrome | Neutropenia | Aneurysm, Abdominal Aortic | Delayed Sleep Phase Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Sclerosing Cholangitis | Portal Vein Thrombosis | Membranous Nephropathy | X-linked Sideroblastic Anemia | Gitelman Syndrome | Hemangioblastoma | Charcot-Marie-Tooth Disease Type 2D | Nephrocalcinosis | Chondrodysplasia Punctata 1, X-linked Recessive | Primary Torsion Dystonia | Thyroid Dysgenesis | MIRAGE Syndrome | Traboulsi Syndrome | Zollinger-Ellison Syndrome | Stroke | Hemochromatosis Type 1 | Mucolipidosis Type II | WAGR Syndrome | Prolactinoma | Diamond-Blackfan Anemia | X-linked Acrogigantism | Chromosome 17q21.31 Deletion Syndrome | Infantile Neuroaxonal Dystrophy | Oculocutaneous Albinism Type 1 | Mucolipidosis | Joubert Syndrome 2 | Hemochromatosis | Asthma, Exercise-induced | Centronuclear Myopathy | Usher Syndrome Type IIC | Spinal Muscular Atrophy Type 2 | Hyperbilirubinemia, Neonatal | Platelet Disorders | Fibrosarcoma | Birk-Barel Syndrome | Thin Basement Membrane Disease | Shprintzen-Goldberg Syndrome | Acute Kidney Injury | Cholestasis, Intrahepatic | Takayasu's Arteritis | Infantile Nephropathic Cystinosis | Aplasia Cutis Congenita | Progressive Encephalopathy-optic Atrophy Syndrome | Huntington's Disease-like 2 | Stroke, Ischemic | Pain | Amyotrophic Lateral Sclerosis | Tonsillitis | Sengers Syndrome | Waardenburg Syndrome Type 2 | Ichthyosis, X-linked | Mandibuloacral Dysplasia With Type A Lipodystrophy | Dominant Optic Atrophy | Progressive Myoclonic Epilepsy | Autosomal Recessive Spastic Paraplegia Type 35 | Cardiac Sarcoidosis | DEND Syndrome