Disease

Frontotemporal Dementia

About the Disease
Frontotemporal Dementia, also known as frontotemporal lobar degeneration, is related to inclusion body myopathy with paget disease of bone and frontotemporal dementia and frontotemporal dementia and/or amyotrophic lateral sclerosis 1, and has symptoms including myoclonus and personality changes. An important gene associated with Frontotemporal Dementia is PSEN1 (Presenilin 1), and among its related pathways/superpathways are Cytoskeletal Signaling and Neuroscience. The drugs Memantine and Citalopram have been mentioned in the context of this disorder. Affiliated tissues include brain, amygdala and bone marrow, and related phenotypes are brain atrophy and visual agnosia

Common Targets
HDAC8 | TMEM106B | CCNF | SPG11 | DYRK1A | KIF13A | C9orf72 | CDK5 | CDK13 | CHRNA7 | HTR2A | IFNL2 | FAM171A2 | GSK3B | PALM2 | SP4 | Neurotrophic Factor (nonspecified subtype) | PSEN2 | COL28A1 | CACNA1C | BTNL2 | ARRB2 | SLC13A4 | JAK2 | LOC107987057 | HNRNPA2B1 | SORT1 | TNIK | G4137 | ZNF532 | LGMN | MOBP | CHCHD10 | CLU | GPR3 | CFAP54 | NDUFS1 | RCOR1 | JAK1 | TSPO | TAF15 | TIA1 | TUBA4A | CRBN | ARRB1 | UNC13A | PRKAG2 | Histone deacetylase (nonspecified subtype) | DAPK1 | USP14 | Amyloid beta A4 precursor protein-binding family (APP-BP) (nonspecified subtype) | MOB3B | MARCHF4 | FOXP2 | ABCC8 | PIKFYVE | APOE | CHMP2B | MMP13 | HAS1 | ABCC9 | TREM2 | BACE1 | GFRA2 | LINC02210-CRHR1 | OPTN | YLPM1 | APP | ALS2 | MAOB | OGA | RAB38 | NUAK1 | GABRA5 | CCDC144NL | G2475 | VCP | PRB1 | RGS6 | Cyclooxygenase (COX) (nonspecified subtype) | PFN1 | ATP9B | CSF1R | ACTN3 | Vacuolar H+ ATPase | G3146 | SCARB2 | FUS | ANG | TNK2 | SMPD3 | DYRK1B | G7124 | HDAC2 | PLEKHH1 | Rho kinase (ROCK) (nonspecified subtype) | HTT | SETX | PRR5L | G6647 | SQLE | ST18 | KCNJ8 | BDNF | FIG4 | HRH3 | NR4A2 | PPARGC1A | GLDN | GRN | CSNK1D | TBK1 | NECTIN2 | SORL1 | ACHE | CDK12 | UBQLN2 | G8878 | TSGA13 | LRRK2 | SNCA | ATXN2 | VPS13C | HDAC1 | WASHC5 | TTBK1 | SMCHD1 | RRBP1 | TRNC | WAKMAR1 | LHFPL3 | LINC01170 | PRNP | L3MBTL1 | SLIT3 | KCNJ11 | RYR1 | WNT3 | TFRC | PLCG2 | GRB2 | SIGMAR1 | Eukaryotic translation initiation factor 2B | MARK2 | CDC7 | LOC105379117 | CHRM1 | EWSR1 | NOS1 | PSEN1 | NF-kappaB (NFkB) | TARDBP | mTOR complex 1 | HDAC3 | Chromosome 16 open reading frame 47 | FLT3 | LRP10

疾病靶点研报
Frontotemporal Dementia

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

Other Diseases

Crimean-Congo Hemorrhagic Fever | Lung Diseases | Spinal And Bulbar Muscular Atrophy | Hypothyroidism | Episodic Ataxia Type 1 | Neurofibromatosis | Essential Fructosuria | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Priapism | Benign Familial Neonatal Convulsions | Restrictive Dermopathy | Hypotrichosis Simplex | Phosphoglycerate Dehydrogenase Deficiency | Twin-to-twin Transfusion Syndrome | Ovarian Hyperstimulation Syndrome | Nephrocalcinosis | Richter's Syndrome | Charcot-Marie-Tooth Disease Type 4D | Constipation | 3-methylglutaconic Aciduria | Primary Pigmented Nodular Adrenocortical Disease | Charcot-Marie-Tooth Disease, Type 6 | Facioscapulohumeral Muscular Dystrophy Type 1 | Treacher Collins Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Meningococcal Infections | Gangliosidosis | Rash | Cabezas Syndrome | Erectile Dysfunction | Peeling Skin Syndrome Type B | Spasticity | Ophthalmia, Sympathetic | Cancer, Kidney | Spinocerebellar Ataxia Type 16 | Charcot-Marie-Tooth Disease | Aceruloplasminemia | Epilepsy Of Infancy With Migrating Focal Seizures | Neuroblastoma | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Panuveitis | Azoospermia | Seborrheic Dermatitis | Usher Syndrome Type III | Scapuloperoneal Myopathy, X-linked Dominant | Woodhouse-Sakati Syndrome | 3-M Syndrome | Chloridorrhea, Congenital | Speech Disorders | Hyperkalemic Periodic Paralysis | Von Hippel-Lindau Disease | Diabetes Insipidus, Neurogenic | Smith-Lemli-Opitz Syndrome | Nicotine Dependence | Biotinidase Deficiency | Paget's Disease Of The Breast | Dystonia Musculorum Deformans | Meier-Gorlin Syndrome | Endometriosis | Noonan Syndrome | Hyperprolactinemia | Hypolipoproteinemia | Rhizomelic Chondrodysplasia Punctata | Trichotillomania | Skin Papilloma | Jalili Syndrome | Pemphigus Vulgaris | Craniofacial Dysostosis | Coronary Heart Disease | Schamberg Disease | Milk Allergy | Myelitis, Transverse | Cirrhosis | Vertigo | Crohn's Disease | Primary Ovarian Insufficiency | Left Ventricular Noncompaction | Chronic Beryllium Disease | Mevalonate Kinase Deficiency | Cartilage Disorders | SAPHO Syndrome | Familial Advanced Sleep Phase Syndrome | Congenital Ichthyosiform Erythroderma | Conn Syndrome | Sarcoidosis | Gastroenteritis | Diabetes Mellitus, Transient Neonatal | Mucolipidosis | Cholesteryl Ester Storage Disease | Keratoacanthoma | Short-chain Acyl-CoA Dehydrogenase Deficiency | Medulloblastoma | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Van Der Knaap Disease | Hodgkin Lymphoma | Early Infantile Epileptic Encephalopathy 4 | Omenn Syndrome | Infertility | Enhanced S-cone Syndrome | Motor Neuron Diseases | Cerebrovascular Disorders | Chondrodysplasia Punctata 2, X-linked Dominant | IgA Deficiency | Crigler-Najjar Syndrome | GLUT1 Deficiency Syndrome | Acne | Congenital Disorders Of Glycosylation | Retinitis | Exostoses | Papilledema | Lymphoma, AIDS-related | Leishmaniasis, Cutaneous | Congenital Poikiloderma | Myofibrillar Myopathy | Keratosis, Actinic | Fibromyalgia | Eiken Syndrome | Sclerocornea | Lattice Corneal Dystrophy | Hyperglycemia | Hepatitis A | Dermatitis | Whipple's Disease | Congenital Dyserythropoietic Anemia Type 1 | Neuroleptic Malignant Syndrome | Lamellar Ichthyosis | Asthma | Cocaine-Related Disorders | Situs Inversus | Adenoid Cystic Carcinoma | Autoimmune Hemolytic Anemia | Granular Corneal Dystrophy | Chronic Granulomatous Disease | Hyperferritinemia-cataract Syndrome | Nephropathy | Chondrodysplasia Punctata | Nutrition Disorders | Becker Muscular Dystrophy | Anorectal Fistula | Bladder Exstrophy | Purpura | Basal Ganglia Disease, Biotin-responsive | Scapuloperoneal Spinal Muscular Atrophy | Myositis | Lafora Disease | Paraganglioma | Congenital Stationary Night Blindness | Endometrial Hyperplasia | Christianson Syndrome | Common Variable Immunodeficiency | Glutaric Aciduria Type 1 | Congenital Adrenal Hyperplasia 1 | Atelosteogenesis Type 1 | Myelomeningocele | Hyperbilirubinemia | Charcot-Marie-Tooth Disease Type 4E | Pneumonia, Mycoplasma | Vogt-Koyanagi-Harada Syndrome | Polycystic Kidney, Autosomal Dominant | Osteochondroma | Wiskott-Aldrich Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Tay-Sachs Disease | Corneal Dystrophy And Perceptive Deafness | Pain | Progressive Osseous Heteroplasia | Mesothelioma, Malignant | Asplenia | Autoimmune Autonomic Ganglionopathy | Hyperkeratosis | Bicuspid Aortic Valve | Distal Myopathy | Amish Infantile Epilepsy Syndrome | MELAS Syndrome | Glaucomatocyclitic Crisis | Heterotaxy | Congenital Bile Acid Synthesis Defect | Non-epidermolytic Palmoplantar Keratoderma | Borjeson-Forssman-Lehmann Syndrome | Hemorrhagic Disorders | Adrenomyeloneuropathy | Chordoma | Hereditary Multiple Exostoses | Bronchitis | Reflex Epilepsy | Gray Platelet Syndrome | Leukoplakia, Oral | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Metanephric Adenoma | Oculocutaneous Albinism Type 1 | Hyperandrogenemia | Iron Metabolism Disorders | Congenital Nystagmus | Osteoporosis-pseudoglioma Syndrome | Mannosidase Deficiency Diseases | Atelosteogenesis Type 2 | Ureteropelvic Junction Obstruction | Chromosome 17q21.31 Deletion Syndrome | Pseudo-pseudohypoparathyroidism | Spinocerebellar Ataxia Type 28 | Genitopatellar Syndrome | Hypoalbuminemia | Infectious Diarrhea | Hypopituitarism | Pyruvate Carboxylase Deficiency Disease | Vasculitis | Bacterial Meningitis | Chronic Mucocutaneous Candidiasis | Herpes Simplex Dermatitis | Basan Syndrome | Roberts Syndrome | Familial Hyperaldosteronism | Long QT Syndrome Type 1 | Cohen Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Hypertension, Pulmonary | Lassa Fever | Glaucoma, Congenital | Mixed Connective Tissue Disease | Congenital Sodium Diarrhea | Phenylketonuria | Common Cold | Hartnup Disease | Leprosy | Robinow Syndrome | Blepharo-cheilo-odontic Syndrome | Hereditary Mixed Polyposis Syndrome | Corneal Edema | Precocious Puberty | Swine Influenza | Kawasaki Disease | Esotropia | Fukuyama Congenital Muscular Dystrophy | Optic Neuritis | Pyruvate Dehydrogenase Deficiency | Pterygium | Sorsby Fundus Dystrophy | Neovascular Glaucoma | Meningioma | Otosclerosis | Blepharoconjunctivitis | Infantile Spasm | Tibial Muscular Dystrophy | Amyloidosis | Dystonia | Adenosine Deaminase 2 Deficiency | Presbyopia | Hepatitis D | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Borderline Personality Disorder | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Melanoma, Uveal | Epilepsy, Generalized | Peyronie's Disease | Retinal Dystrophy, Early-onset Severe | Saul-Wilson Syndrome | Melnick-Needles Syndrome | Stevens-Johnson Syndrome | Sick Sinus Syndrome 1 | Spitzoid Melanoma | Lentigo | Pyruvate Kinase Deficiency | Agranulocytosis | Multisystemic Smooth Muscle Dysfunction Syndrome | Keratosis | Tularemia | Spinocerebellar Ataxia Type 15 | Okihiro Syndrome | Brachial Plexus Neuropathy | Nicolaides-Baraitser Syndrome | Encephalopathy | Stomatitis | Hemochromatosis | Leigh Syndrome | LMNA-related Congenital Muscular Dystrophy | Megaloblastic Anemia | Bloom Syndrome | Familial Exudative Vitreoretinopathy | Hereditary Spastic Paraplegia | Neurocutaneous Syndromes | Actinomycetoma | Microphthalmia, Syndromic 7 | Usher Syndrome Type I | Urea Cycle Disorder | Frontometaphyseal Dysplasia | Choroiditis | Spinocerebellar Ataxia Type 42 | Schwartz-Jampel-Aberfeld Syndrome | Heimler Syndrome | Yellow Fever | Prolidase Deficiency | Tetanus | Early Infantile Epileptic Encephalopathy 1 | Asperger Syndrome | Basal Ganglia Disease | Spinocerebellar Ataxia Type 40 | Dermatomyositis | Pouchitis | Arts Syndrome | Hyperparathyroidism | Chordoid Glioma | VACTERL/VATER Association | Chronic Myeloid Leukemia | Hyperoxaluria | Rubinstein-Taybi Syndrome | Myoclonus | Progressive Familial Intrahepatic Cholestasis Type 3 | Glaucoma | Retinal Telangiectasia | Farber Disease | Congenital Muscular Dystrophy | Intellectual Disability, Autosomal Dominant 5 | Hypermethioninemia | Androgenic Alopecia | DOCK8 Immunodeficiency Syndrome | Herpes Genitalis | Chitayat Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Arthritis, Psoriatic | Cardiomyopathy, Restrictive | B-cell Prolymphocytic Leukemia | Blood Protein Disorders | REM Sleep Behavior Disorder | Neuronal Ceroid Lipofuscinosis | Myasthenia Gravis | Hereditary Sensory Neuropathy Type 1 | Loeys-Dietz Syndrome | Waardenburg Syndrome Type 2A | Thrombotic Microangiopathy | Cutis Laxa | Relapsing Polychondritis | Osteogenesis Imperfecta Type IV | Generalized Epilepsy And Paroxysmal Dyskinesia | Thyroid Dysgenesis | Kabuki Syndrome | Glycogen Storage Disease Type 5 | Charcot-Marie-Tooth Disease Type 2D | Pseudohypoparathyroidism Type 1A | Hypocalcemia | Lichen Sclerosus | Scabies | ICF Syndrome | Silver-Russell Syndrome | Acute Myeloid Leukemia | Spinocerebellar Ataxia Type 31 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Epidermolysis Bullosa Dystrophica | Cerebellar Ataxia, Cayman Type | Bursitis | Focal Facial Dermal Dysplasia | Thromboembolism | Alzheimer Disease, Late Onset | Diabetic Encephalopathy | Leukemia | Distal Myopathy 2 | Diverticulitis | Combined Malonic And Methylmalonic Acidemia | Liver Failure, Acute Infantile | Neurofibromatosis Type 2 | Learning Disability | Pneumonia, Bacterial | Primrose Syndrome | Schizophrenia, Paranoid | Rickets | Juvenile Xanthogranuloma | Cholestasis | Pituitary Disorders | Waardenburg Syndrome Type 4A | Epidermolysis Bullosa Acquisita | Angiomyolipoma | Parvovirus B19 Infection | Tendinopathy | Torticollis | Choroideremia | CREST Syndrome | Onchocerciasis | Cancer, Skin | Genee-Wiedemann Syndrome | Vitreoretinal Degeneration, Snowflake Type | Pseudoexfoliation Syndrome | Cryoglobulinemia | CHARGE Syndrome | Prolactinoma | AIDS Dementia Complex | Pierpont Syndrome | Lateral Meningocele Syndrome | Haim-Munk Syndrome | Lymphoma | Saethre-Chotzen Syndrome | Hyperostosis | Dengue Shock Syndrome | Babesiosis | Lymphedema | Schwannoma | Paraplegia | Chronic Kidney Disease | Inflammatory Joint Disease | Seizures-scoliosis-macrocephaly Syndrome | Cystitis, Interstitial | Alkaptonuria