Disease

Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex

About the Disease
Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1, also known as guam disease, is related to frontotemporal dementia and/or amyotrophic lateral sclerosis 3 and frontotemporal dementia and/or amyotrophic lateral sclerosis 2, and has symptoms including tremor, bradykinesia and abnormality of extrapyramidal motor function. An important gene associated with Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 is TRPM7 (Transient Receptor Potential Cation Channel Subfamily M Member 7), and among its related pathways/superpathways are Neuroscience and Copper homeostasis. The drugs Varenicline and Riluzole have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, spinal cord and brain, and related phenotypes are muscle weakness and dementia

Common Targets
MATR3 | LMNB1 | PARK7

疾病靶点研报
Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex

Note: If you'd like to get a target analysis report for Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex, 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 Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Parkinsonism | Uterine Leiomyoma | Early Infantile Epileptic Encephalopathy 4 | Optic Neuropathy | Hyperkalemic Periodic Paralysis | Batten Disease | Fuchs Heterochromic Iridocyclitis | Endometritis | Reflex Epilepsy | Rheumatoid Arthritis | Paroxysmal Kinesigenic Dyskinesia | Fanconi Anemia | Hyperlipidemia, Familial Combined | Apraxia | Neovascular Glaucoma | Glaucoma | Corneal Edema | Glycogen Storage Disease Type 6 | Congenital Aniridia | Mast Cell Leukemia | Cholelithiasis | Klippel-Feil Syndrome | Uremic Pruritus | Porphyria | Optic Nerve Diseases | Yellow Fever | Aplasia Cutis Congenita | IMAGe Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Hyperacusis | Carbohydrate Metabolism Disorders | Schnyder Crystalline Corneal Dystrophy | Meconium Ileus | Pemphigus | Hyperthyroidism | Epidermolysis Bullosa Simplex | Hyperinsulinemia | Optic Neuritis | Retinopathy Of Prematurity | Ehlers-Danlos Syndrome | Tinea Versicolor | Cholestasis | Trigonocephaly | Cancer, Brain | Patent Foramen Ovale | Nephropathy | Early Infantile Epileptic Encephalopathy 28 | Camurati-Engelmann Disease | Inflammatory Myofibroblastic Tumor | Prolymphocytic Leukemia | Tendinitis | Hepatic Steatosis | Acrodysostosis | Sialoadenitis | Persistent Truncus Arteriosus | Neurofibroma, Plexiform | Peeling Skin Syndrome Type B | Renal Failure | Emery-Dreifuss Muscular Dystrophy | Antisocial Personality Disorder | Progressive Familial Intrahepatic Cholestasis Type 2 | Hyperoxaluria | Iron Overload | Lipodystrophy | Okihiro Syndrome | Dysfibrinogenemia | Atherosclerosis | Acrodermatitis | Fibromyalgia | Spinocerebellar Ataxia Type 7 | Meckel-Gruber Syndrome | Lymphoproliferative Disease, X-linked | Phenylketonuria | Combined Deficiency Of Factor V And Factor VIII | Turner's Syndrome | Encephalitis, Tick-borne | Pupil Disorders | Wieacker-Wolff Syndrome | Long QT Syndrome Type 1 | Christianson Syndrome | Tuberculosis | Duchenne Muscular Dystrophy | T-cell Leukemia | Chronic Granulomatous Disease | Cellulitis | Amyotrophic Lateral Sclerosis, Juvenile | McCune-Albright Syndrome | Micro Syndrome | Glomerulonephritis, Membranous | Cardiofaciocutaneous Syndrome | Idiopathic Pulmonary Fibrosis | Erythema Nodosum | Urethritis | Tularemia | Sarcoma | Contact Dermatitis | Craniofacial Dysostosis | Osteogenesis Imperfecta Type IV | Lymphedema | Spastic Paraplegia Type 7 | Retinitis Pigmentosa | Dystrophy, Cone-rod | Keratosis, Seborrheic | Blood Protein Disorders | Renal Hypomagnesemia 3 | Double Outlet Right Ventricle | Intracranial Hypertension | Auriculocondylar Syndrome | Hypertension, Portal | Methylmalonic Acidemia | Congenital Generalized Lipodystrophy | Smith-Magenis Syndrome | Mixed Connective Tissue Disease | Veno-occlusive Disease | Herpes Genitalis | Ophthalmia, Sympathetic | Myoclonic Epilepsy With Ragged Red Fibers | Pontocerebellar Hypoplasia Type 7 | Cerebellar Ataxia, Cayman Type | Cherubism | Rhabdomyosarcoma, Embryonal | Diabetes Type 2 | Dominant Optic Atrophy | Krabbe Disease | Retinopathy, Diabetic | Thrombosis | Renal Dysplasia | Spinocerebellar Ataxia Type 1 | Vasculitis | Left Ventricular Noncompaction | Supravalvular Aortic Stenosis | Congenital Hereditary Endothelial Dystrophy Type I | Light Chain Amyloidosis | Iron Deficiency Anemia | Bicuspid Aortic Valve | Carcinoma In Situ | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Raine Syndrome | Galloway-Mowat Syndrome | Congenital Central Hypoventilation Syndrome | Charcot-Marie-Tooth Disease Type 2D | Mucolipidosis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Progressive Myoclonic Epilepsy | Senior-Loken Syndrome | ADNP Syndrome | Intestinal Tuberculosis | Hypereosinophilic Syndrome | Acne Vulgaris | Granular Corneal Dystrophy Type 1 | Spondylolisthesis | Hyper IgE Syndrome | Lupus Erythematosus | Joubert Syndrome 2 | Spinocerebellar Ataxia Type 21 | Nicolaides-Baraitser Syndrome | Language Disorders | Hypertelorism | Cardiomyopathy, Restrictive | Spinocerebellar Ataxia Type 38 | Paternal Uniparental Disomy Of Chromosome 14 | Mohr-Tranebjaerg Syndrome | Choriocarcinoma | Persistent Mullerian Duct Syndrome | Woodhouse-Sakati Syndrome | Teratozoospermia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Retinal Coloboma | Polycystic Kidney, Autosomal Dominant | Antiphospholipid Syndrome | Gastrointestinal Disorders | Wolcott-Rallison Syndrome | Progressive Familial Intrahepatic Cholestasis Type 1 | Acute Lung Injury | Pityriasis Rubra Pilaris | Hyperuricemic Nephropathy, Familial Juvenile | Cole-Carpenter Syndrome | Peripheral Neuropathy | Hydrops Fetalis | Skin Fragility-woolly Hair Syndrome | Neural Tube Defect | Transcobalamin Deficiency | Sclerocornea | Acne | Camptocormia | Thyroid Hormone Resistance | Crigler-Najjar Syndrome | Kindler Syndrome | Irritable Bowel Syndrome | Polyarteritis Nodosa | Growth Hormone Excess | Hypertension, Renovascular | Panic Disorder | Intestinal Pseudo-obstruction | Cousin Syndrome | Alzheimer Disease, Late Onset | Neuropathy | Bardet-Biedl Syndrome | Waardenburg Syndrome Type 1 | Nance-Horan Syndrome | Multiple Sclerosis, Secondary Progressive | Short-chain Acyl-CoA Dehydrogenase Deficiency | Meningococcal Infections | Ollier Disease | Zygomycosis | Idiopathic Multicentric Castleman Disease | Cramp Fasciculation Syndrome | Juvenile Hyaline Fibromatosis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Dengue Hemorrhagic Fever | Neuroectodermal Tumors, Primitive | Hyperinsulinemic Hypoglycemia | Hidradenitis Suppurativa | Nestor-Guillermo Progeria Syndrome | Glycogen Storage Disease Type 3 | Non-Langerhans Cell Histiocytosis | Dyslipidemia | Subcortical Band Heterotopia | Autism | Uveitis, Anterior | Neurocysticercosis | Bruck Syndrome | Niemann-Pick Disease | Myelitis, Transverse | Mevalonate Kinase Deficiency | Pseudomyxoma Peritonei | Spinocerebellar Ataxia Type 40 | Conn Syndrome | Central Core Disease | Familial Partial Lipodystrophy | Lymphoma Lymphoblastic | Lissencephaly 2 | Obesity | Meningococcal Meningitis | Pseudohypoparathyroidism Type 1A | Spinocerebellar Ataxia Type 12 | Hereditary Xerocytosis | Mitochondrial Myopathy | Hepatitis B, Chronic | Blue Rubber Bleb Nevus Syndrome | Premenstrual Syndrome | GNE Myopathy | Neurofibromatosis-Noonan Syndrome | Scleritis | Nephroblastoma | Major Depression | Anal Fissure | Hemochromatosis Type 2 | N-acetylglutamate Synthase Deficiency | Chronic Lymphocytic Leukemia | Pancreatitis, Chronic | Acute Motor Axonal Neuropathy | Malaria, Cerebral | Partington Syndrome | Episodic Ataxia | DEND Syndrome | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Rhinitis | Duodenal Atresia | Keratoconjunctivitis | Bare Lymphocyte Syndrome | Autosomal Recessive Congenital Ichthyosis | Echinococcosis | Hypervalinemia | Lattice Corneal Dystrophy Type 1 | Liebenberg Syndrome | H Syndrome | Adenocarcinoma | Hemophagocytic Lymphohistiocytosis | Precocious Puberty | Autosomal Recessive Spastic Paraplegia Type 54 | Sporadic Inclusion Body Myositis | Frontotemporal Dementia | Familial Episodic Pain Syndrome | Thromboembolism | Impetigo | Knobloch Syndrome | Malnutrition | Non-proliferative Diabetic Retinopathy | Tangier Disease | Microtia | Odonto-onycho-dermal Dysplasia | Pleomorphic Xanthoastrocytoma | Glomerulonephritis, Membranoproliferative | Ocular Surface Squamous Neoplasia | Protein C Deficiency | Lung Diseases | Hoyeraal-Hreidarsson Syndrome | Asphyxia Neonatorum | Pontocerebellar Hypoplasia | Jaundice, Obstructive | Osteogenesis Imperfecta | Xeroderma Pigmentosum Variant Type | Enterocolitis, Necrotizing | Tardive Dyskinesia | Ichthyosis | Dystonia Musculorum Deformans | B-cell Chronic Lymphocytic Leukemia | Agranulocytosis | Scapuloperoneal Spinal Muscular Atrophy | Myotonic Disorders | Stomatitis | Agammaglobulinemia | Constipation | Arteriosclerosis | Palmoplantar Keratoderma | Pneumoconiosis | 5-oxoprolinase Deficiency | Aldosteronism | Sjogren Syndrome | Sponastrime Dysplasia | Fetal Akinesia Deformation Sequence | Anuria | Multiple Sulfatase Deficiency | Autoimmune Polyendocrinopathy Syndrome Type I | Leukemia-lymphoma, Adult T-cell | Meningioma | Neurofibroma | Gastritis | Paget's Disease Of The Breast | Acute Chest Syndrome | Fabry's Disease | Filariasis | Anovulation | Blepharoconjunctivitis | Cornelia De Lange Syndrome | Osteosclerosis | Trichuriasis | Posterior Polar Cataract | Pyloric Stenosis, Infantile Hypertrophic | Neuromyotonia | Prostatitis | Viral Meningitis | Japanese Encephalitis | Perivascular Epithelioid Cell Tumor | Neurogenic Bladder | Gastritis, Atrophic | Usher Syndrome Type IIC | Granuloma Annulare | Leber Hereditary Optic Neuropathy | IgA Nephropathy | Endophthalmitis | Lymphoproliferative Disorders | Histoplasmosis | Omenn Syndrome | Stromal Corneal Dystrophy | Silicosis | Campomelic Dysplasia | Macrodactyly | Oligospermia | Stroke, Hemorrhagic | Traboulsi Syndrome | Chromosome 8q21.11 Deletion Syndrome | Walker-Warburg Syndrome | Hereditary Mixed Polyposis Syndrome | Granular Corneal Dystrophy | Pterygium | Tenosynovial Giant Cell Tumor | Salla Disease | Hepatic Veno-occlusive Disease | Keratoconus | Gangliosidosis | Hydrocephalus | Hypohidrotic Ectodermal Dysplasia, X-linked | Cutis Laxa | Mitochondrial Disease | Congenital Poikiloderma | Erectile Dysfunction | Retinal Telangiectasia | Epithelial-myoepithelial Carcinoma | Schistosomiasis Mansoni | Diffuse Palmoplantar Keratoderma | Primary Biliary Cholangitis | Hypersensitivity | Lathosterolosis | Disseminated Intravascular Coagulation | Cataplexy | Aldosterone Synthase Deficiency | Cystinosis | Diastrophic Dysplasia | Urolithiasis | Benign Familial Neonatal Convulsions | Pelvic Inflammatory Disease | Wiedemann-Steiner Syndrome | Waardenburg Syndrome | Motor Neuron Diseases | Centronuclear Myopathy | Familial Cerebral Amyloid Angiopathy | Mucormycosis | Ischemia | Mitochondrial DNA Depletion Syndrome | Conjunctivitis | Niemann-Pick Disease, Type C | Splenomegaly | Adrenal Insufficiency | Hypokalemia | Hemophilia | Abetalipoproteinemia | Compartment Syndrome | Canavan Disease