Disease

Primary Progressive Nonfluent Aphasia

About the Disease
Progressive Non-Fluent Aphasia, also known as progressive nonfluent aphasia, is related to frontotemporal lobar degeneration with tdp43 inclusions, grn-related and echolalia. An important gene associated with Progressive Non-Fluent Aphasia is PSEN1 (Presenilin 1), and among its related pathways/superpathways are Neuroscience and Cytoskeletal Signaling. The drugs Aluminum hydroxide and Corticosterone have been mentioned in the context of this disorder. Affiliated tissues include brain, skin and caudate nucleus, and related phenotypes are thickened nuchal skin fold and memory impairment

Common Targets
G4137 | TREM2 | GRN | APOE | EWSR1

疾病靶点研报
Primary Progressive Nonfluent Aphasia

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

Other Diseases

Norrie Disease | Thyroiditis, Autoimmune | Neurofibromatosis-Noonan Syndrome | Osteoglophonic Dysplasia | Neuronal Ceroid Lipofuscinosis | Carpal Tunnel Syndrome | Rubinstein-Taybi Syndrome | Borderline Personality Disorder | Specific Granule Deficiency | Hypertension, Portal | Fibrosis | Diastrophic Dysplasia | Chloridorrhea, Congenital | Noonan Syndrome | Chordoma | Alpha-mannosidosis | Neurocutaneous Syndromes | Lipid Storage Diseases | Ichthyosis, X-linked | Kabuki Syndrome | Lupus Erythematosus | Loeys-Dietz Syndrome | Urea Cycle Disorder | Portal Vein Thrombosis | Ollier Disease | Marshall-Smith Syndrome | Microcephaly | Cardiospondylocarpofacial Syndrome | Herpes Genitalis | Jacobsen Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Neuroectodermal Tumors, Primitive | Systemic Lupus Erythematosus | Lymphopenia | Lipodystrophy | Aromatic L-amino Acid Decarboxylase Deficiency | Renal Tubular Dysgenesis | Apparent Mineralocorticoid Excess Syndrome | MELAS Syndrome | Dwarfism | Pemphigus Foliaceus | Cryoglobulinemia | Craniometaphyseal Dysplasia | Nail-Patella Syndrome | Spinocerebellar Ataxia Type 17 | Trichotillomania | Schizoaffective Disorder | Guttate Psoriasis | Glaucoma, Congenital | Liddle Syndrome | Primary Progressive Nonfluent Aphasia | Amyotrophic Lateral Sclerosis | Leri-Weill Dyschondrosteosis | Hypercalcemia | Kaposiform Hemangioendothelioma | Hyperekplexia | Waardenburg Syndrome Type 2E | Epidermolytic Hyperkeratosis | Spinocerebellar Ataxia Type 40 | Hepatitis A | Rickets | VACTERL/VATER Association | Papilloma | Clouston Hidrotic Ectodermal Dysplasia | Glutaric Aciduria Type 1 | Roberts Syndrome | Extramammary Paget's Disease | Angiomyolipoma | Schizophrenia | Waardenburg Syndrome Type 4A | Granular Corneal Dystrophy Type 1 | Protein C Deficiency | Graft-versus-host Disease | Cavitary Optic Disc Anomalies | Renal Dysplasia | Tyrosinemia | Schaaf-Yang Syndrome | Smoldering Myeloma | Cleidocranial Dysplasia | Distal Myopathy | Macrophage Activation Syndrome | Multiple System Atrophy | McLeod Syndrome | KBG Syndrome | Rolandic Epilepsy | Intracerebral Hemorrhage | Charcot-Marie-Tooth Disease, Type 2C | Chondromyxoid Fibroma | Peeling Skin Syndrome Type B | Gastroenteritis, Eosinophilic | Hereditary Elliptocytosis | Proximal Symphalangism | Congenital Stationary Night Blindness | Hermansky-Pudlak Syndrome | Osteochondrosis | Carcinoma, Signet Ring Cell | Skin Fragility-woolly Hair Syndrome | Myocarditis | Non-Hodgkin Lymphoma | Ophthalmia, Sympathetic | Seizures | Rhabdomyosarcoma, Alveolar | Lipid Metabolism Disorders | Hartnup Disease | Sick Sinus Syndrome 1 | Urolithiasis | Nail Disorder, Nonsyndromic Congenital | Snyder-Robinson Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Cryptosporidiosis | Keratoacanthoma | Gestational Trophoblastic Disease | Diabetes Insipidus, Neurogenic | Papulopustular Rosacea | Epidermolytic Palmoplantar Keratoderma | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Macrodactyly | Tetanus | Chylothorax, Congenital | Glycogen Storage Disease Type 6 | Spinocerebellar Ataxia Type 1 | Argininosuccinic Aciduria | Spinal And Bulbar Muscular Atrophy | Pseudomyxoma Peritonei | Neurofibroma | Acrocallosal Syndrome | Pseudoexfoliation Syndrome | Esthesioneuroblastoma | Milk Allergy | Pilomatrix Carcinoma | Axenfeld-Rieger Syndrome | Poikiloderma With Neutropenia | Usher Syndrome Type IIC | Benign Familial Infantile Seizures | Ganglioneuroma | Esophagitis, Eosinophilic | Hydrolethalus Syndrome | Hemochromatosis Type 2 | Partington Syndrome | Bronchitis, Chronic | Anti-glomerular Basement Membrane Disease | Swine Influenza | Zellweger Syndrome | Sarcoidosis, Pulmonary | Progressive Familial Intrahepatic Cholestasis Type 1 | Pseudohypoparathyroidism Type 1A | Periodic Limb Movement Disorder | Currarino Syndrome | Pseudo-pseudohypoparathyroidism | Anorchia | Lymphoma, Follicular | Anthrax | Borjeson-Forssman-Lehmann Syndrome | Skin Papilloma | Periodontitis | Common Cold | Retinal Diseases | Wiskott-Aldrich Syndrome | Gardner Syndrome | Wiedemann-Steiner Syndrome | McCune-Albright Syndrome | Lateral Meningocele Syndrome | Epidermolysis Bullosa Dystrophica | Pseudohermaphroditism | Abetalipoproteinemia | VEXAS Syndrome | Neutrophilia | Cellulitis | Creutzfeldt-Jakob Disease | Fibromyalgia | Infectious Diarrhea | Chromosome 5q Deletion Syndrome | Infantile Spasm | Multiple Hamartoma Syndrome | Lymphangioleiomyomatosis | T-cell Leukemia | Uremic Pruritus | Pterygium | Combined Malonic And Methylmalonic Acidemia | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Trichothiodystrophy | Dermatomyositis | Histoplasmosis | Interstitial Lung Diseases | Lymphoma, B-cell | Erectile Dysfunction | Methemoglobinemia | Brachydactyly | Wolfram Syndrome | Adenylosuccinate Lyase Deficiency | Polycythemia Vera | DNA Ligase IV Deficiency | Dyslipidemia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Urticaria | Heterotopic Ossification | Hereditary Hemorrhagic Telangiectasia Type 2 | Blue Rubber Bleb Nevus Syndrome | Pneumonia, Mycoplasma | Split Hand-foot Malformation | Disseminated Intravascular Coagulation | Adenomatoid Tumor | Scleroderma, Diffuse | Myotonic Disorders | Prostatitis | Granular Corneal Dystrophy | Optic Neuritis | Iron Metabolism Disorders | Hemophagocytic Lymphohistiocytosis | Krabbe Disease | Choriocarcinoma | Pyruvate Kinase Deficiency | Aldosterone Deficiency | Hemorrhagic Disorders | CHARGE Syndrome | Glycogen Storage Disease Type 0 | Ellis-Van Creveld Syndrome | Lichen Planus | Mitochondrial DNA Depletion Syndrome 13 | Otosclerosis | Spondylolisthesis | Chorea-acanthocytosis | GAPO Syndrome | Infertility, Male | Insulin Resistance | Bainbridge-Ropers Syndrome | Hyperparathyroidism | Rhabdomyosarcoma | Erythropoietic Protoporphyria | Scapuloperoneal Spinal Muscular Atrophy | Asperger Syndrome | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Kidney Stones | Glycogen Storage Disease Type 9 | Macrophagic Myofasciitis | Pityriasis Rubra Pilaris | Menetrier Disease | Charcot-Marie-Tooth Disease Type 2E | Cutaneous Lupus Erythematosus | Congenital Primary Aphakia | Acne | Myocardial Infarction | Glutathione Synthetase Deficiency | Dent Disease | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Arts Syndrome | Dowling-Degos Disease | Birk-Barel Syndrome | Retinopathy Of Prematurity | Hyperkalemic Periodic Paralysis | Chondroma | Corneal Dystrophies, Hereditary | Spondylocarpotarsal Synostosis Syndrome | Neurofibroma, Plexiform | Schistosomiasis | Eosinophilia | Multiple Sclerosis, Secondary Progressive | Porphyria Cutanea Tarda | Encephalopathy, Hepatic | Cutaneous Angiosarcoma | Sleep Apnea, Obstructive | WAGR Syndrome | Wolman Disease | Osteonecrosis | Intestinal Hypomagnesemia 1 | Aicardi-Goutieres Syndrome | Acute Coronary Syndrome | Martsolf Syndrome | Myosin Storage Myopathy | HUPRA Syndrome | Congenital Stromal Corneal Dystrophy | Schizotypal Personality Disorder | Pleural Tuberculosis | Esotropia | Intermittent Claudication | Progressive Familial Intrahepatic Cholestasis | Robinow Syndrome | Glomerulonephritis | Diabetes Type 2 | Coffin-Lowry Syndrome | Dentinogenesis Imperfecta | Hypotrichosis Simplex | Cabezas Syndrome | Multiple Sclerosis, Primary Progressive | Yellow Fever | Pneumonia, Viral | Spinocerebellar Ataxia Type 3 | Succinic Semialdehyde Dehydrogenase Deficiency | Inflammatory Myofibroblastic Tumor | Neutropenia | Schnyder Crystalline Corneal Dystrophy | Arthritis, Gouty | Stroke | Metaphyseal Chondrodysplasia, Schmid Type | Leukemia | Thanatophoric Dysplasia Type 1 | Oral Lichen Planus | Nasodigitoacoustic Syndrome | Neovascular Glaucoma | Growth Hormone Excess | N-acetylglutamate Synthase Deficiency | Hypersensitivity Pneumonitis | Sweet Syndrome | Cocaine-Related Disorders | Blastomycosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Astrocytoma, Anaplastic | Spinocerebellar Ataxia Type 7 | Hypotrichosis | Bone Giant Cell Tumor | Stevens-Johnson Syndrome | Renal-hepatic-pancreatic Dysplasia | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Lattice Corneal Dystrophy | Unverricht-Lundborg Syndrome | Heart Septal Defects | Epidermodysplasia Verruciformis | Dysgerminoma | ADNP Syndrome | Oculodentodigital Dysplasia | ACTH-independent Macronodular Adrenal Hyperplasia | Fundus Albipunctatus | Scapuloperoneal Myopathy, X-linked Dominant | Achromatopsia | Intestinal Pseudo-obstruction | Polycystic Kidney, Autosomal Recessive | Polyradiculopathy | Crohn's Disease | LMNA-related Congenital Muscular Dystrophy | Bruck Syndrome | Diabetic Neuropathy | Hyperthermia, Malignant | Vitreoretinopathy, Proliferative | Brooke-Spiegler Syndrome | Gigantism | Cryptococcal Meningitis | Asthma, Exercise-induced | Hyperprolactinemia | Oculopharyngeal Muscular Dystrophy | Saethre-Chotzen Syndrome | Autosomal Recessive Bestrophinopathy | Tylosis With Esophageal Cancer | Congenital Ichthyosiform Erythroderma | Waardenburg Syndrome Type 4 | Smith-Lemli-Opitz Syndrome | Congenital Heart Defects | Cheilitis | Nephrosclerosis | Ichthyosis Bullosa Of Siemens | Adenoid Cystic Carcinoma | Walker-Warburg Syndrome | Sarcomatoid Carcinoma Of The Lung | Ichthyosis Hystrix, Curth-Macklin Type | Aldosterone Synthase Deficiency | Stroke, Ischemic | Silver-Russell Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Metabolic Diseases | Spinocerebellar Ataxia Type 16 | Cholesteryl Ester Storage Disease | Early Infantile Epileptic Encephalopathy 28 | Marfan Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Pompe Disease | Hamartoma | Spasticity | Pheochromocytoma | Aspergillosis | Amebiasis | Tricho-hepato-enteric Syndrome | Retinoblastoma | Diabetic Nephropathy | Hemorrhoids | Enterocolitis, Necrotizing | Pre-eclampsia | Sickle Cell Anemia | Nicolaides-Baraitser Syndrome | Diabetes Mellitus, Transient Neonatal | Turner's Syndrome | Hereditary Sensory Neuropathy Type 1 | Shock, Cardiogenic | Ataxia-ocular Apraxia 2 | Acute Chest Syndrome | Acromicric Dysplasia | Occipital Neuralgia | Leukoplakia, Oral | Lesch-Nyhan Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Otitis Externa | Dementia, Vascular | Carbohydrate Metabolism Disorders | Osteogenesis Imperfecta Type VI | Parapsoriasis | Ectopia Lentis, Isolated, Autosomal Recessive | Paraplegia | Hemochromatosis Type 1 | Leukoencephalopathy, Progressive Multifocal | Migraine | Mandibuloacral Dysplasia With Type A Lipodystrophy | Rheumatic Heart Disease