Disease

Autoimmune Autonomic Ganglionopathy

About the Disease
Autoimmune Autonomic Ganglionopathy, also known as autoimmune autonomic neuropathy, is related to dysautonomia and autonomic nervous system disease. The drugs gamma-Globulins and Antibodies have been mentioned in the context of this disorder. Affiliated tissues include lung.

Common Targets
CHRNA3

疾病靶点研报
Autoimmune Autonomic Ganglionopathy

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

Other Diseases

Vertebrobasilar Insufficiency | Familial Exudative Vitreoretinopathy | Rhabdomyosarcoma | Lipid Metabolism Disorders | Fukuyama Congenital Muscular Dystrophy | Postpartum Depression | Hypobetalipoproteinemias | Renal Hypouricemia | Spinocerebellar Ataxia Type 10 | Chronic Neutrophilic Leukemia | Diffuse Intrinsic Pontine Glioma | Membranous Nephropathy | Acute Myeloid Leukemia | Dowling-Degos Disease | Choriocarcinoma | DOCK8 Immunodeficiency Syndrome | Myelitis | Traboulsi Syndrome | Pompe Disease | Fundus Albipunctatus | Sick Sinus Syndrome | Sulfite Oxidase Deficiency | Renal Tubular Acidosis | Hypohidrotic Ectodermal Dysplasia, X-linked | Chiari Malformation Type I | Cystitis | Hereditary Spherocytosis | Spondylometaphyseal Dysplasia | Arthritis, Reactive | Systemic Mastocytosis | Pneumothorax | Peutz-Jeghers Syndrome | Myocarditis | D-2-Hydroxyglutaric Aciduria | Trachoma | Trigonocephaly | Mucolipidosis | Creatine Deficiency Syndrome Due To AGAT Deficiency | LEOPARD Syndrome | Transient Bullous Dermolysis Of The Newborn | Nestor-Guillermo Progeria Syndrome | Axenfeld-Rieger Syndrome | Premenstrual Syndrome | Portal Vein Thrombosis | Gallstones | Ganglioglioma | Giant Axonal Neuropathy | Marinesco-Sjogren Syndrome | Inflammatory Bowel Disease | Migraine | Joubert Syndrome | Dystonia Musculorum Deformans | Snyder-Robinson Syndrome | Early Infantile Epileptic Encephalopathy 4 | Liver Diseases | Beta-Propeller Protein-associated Neurodegeneration | Glycogen Storage Disease Type 3 | Cushing Syndrome | Cryoglobulinemia | Biotinidase Deficiency | Insulinoma | Glycogen Storage Disease Type 4 | Sporadic Inclusion Body Myositis | Intestinal Hypomagnesemia 1 | Muscle Wasting | Bacterial Meningitis | Renal-hepatic-pancreatic Dysplasia | Trichotillomania | Pulmonary Alveolar Microlithiasis | Hypereosinophilic Syndrome | Hypodontia | Tatton-Brown-Rahman Syndrome | Extramammary Paget's Disease | Neurodegeneration With Brain Iron Accumulation | Arrhythmogenic Right Ventricular Cardiomyopathy | Galloway-Mowat Syndrome | Yellow Fever | Acrocallosal Syndrome | Coronary Artery Disease | Pseudohypoaldosteronism | Myelitis, Transverse | Congenital Myasthenic Syndrome | Cutaneous Angiosarcoma | Retinoblastoma | Chorea-acanthocytosis | Alexander Disease | Multicentric Carpotarsal Osteolysis Syndrome | Spinocerebellar Ataxia Type 42 | Hypercalcemia | Paracoccidioidomycosis | Currarino Syndrome | Connective Tissue Disorders | Primary Carnitine Deficiency | Primary Torsion Dystonia | Bronchiolitis | Optic Nerve Diseases | Diverticulitis | Amenorrhea | Cancer, Bladder | Malnutrition | Sertoli Cell-only Syndrome | Congenital Heart Defects | Ovarian Hyperstimulation Syndrome | Preaxial Polydactyly | Hypertension, Renovascular | Vitreoretinal Degeneration, Snowflake Type | Sarcosinemia | Learning Disability | Pyruvate Decarboxylase Deficiency | Familial Advanced Sleep Phase Syndrome | Angioimmunoblastic T-cell Lymphoma | Chronic Myelomonocytic Leukemia | Diabetes Gestational | Beckwith-Wiedemann Syndrome | Panic Disorder | Microtia | Inflammatory Myofibroblastic Tumor | Ellis-Van Creveld Syndrome | Agoraphobia | Progressive External Ophthalmoplegia | Parvovirus B19 Infection | Hereditary Sensory Neuropathy Type 1 | Blastomycosis | Myoclonic Epilepsy With Ragged Red Fibers | Muckle-Wells Syndrome | Sezary Syndrome | Seborrheic Dermatitis | Chromosome 5q Deletion Syndrome | Autoimmune Disease | Carcinoma, Squamous Cell | Leigh Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Synovitis | Pulverulent Zonular Cataract | Long QT Syndrome Type 1 | Arthritis, Gouty | Osteogenesis Imperfecta | Wiskott-Aldrich Syndrome | Pelvic Inflammatory Disease | Macular Corneal Dystrophy | Thrombotic Microangiopathy | Bloom Syndrome | Leiomyosarcoma | Zygomycosis | Persistent Mullerian Duct Syndrome | Granular Corneal Dystrophy | Adrenal Insufficiency | Hidradenitis Suppurativa | Uremic Pruritus | Vogt-Koyanagi-Harada Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Desmosterolosis | Porokeratosis | Glioma | Gardner Syndrome | Japanese Encephalitis | Glioblastoma Multiforme | Inflammatory Myopathy | Systemic Lupus Erythematosus | Left Ventricular Noncompaction | Hereditary Multiple Exostoses | Corticobasal Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Osteopetrosis | Dystonia | Diabetes | Congenital Tufting Enteropathy | Histoplasmosis | Huntington's Disease-like 2 | Tibial Muscular Dystrophy | Coffin-Siris Syndrome | Neural Tube Defect | Acrodysostosis | Burn-McKeown Syndrome | Cutaneous T-cell Lymphoma | Carcinoma In Situ | Cutaneous Lupus Erythematosus | Pontocerebellar Hypoplasia | Blastoma, Pleuropulmonary | Klinefelter Syndrome | Vasculitis | Pathological Gambling | Zellweger Syndrome | Sarcoidosis | Onchocerciasis | Sleep Disorder | Periventricular Leukomalacia | Astrocytoma | Aldosterone Synthase Deficiency | Dysthymia | Cancer, Brain | Smith-Kingsmore Syndrome | Norrie Disease | Gilbert Syndrome | Sleep Apnea, Central | Kindler Syndrome | Acute Leukemia | Juvenile Myoclonic Epilepsy | Vitamin B12 Deficiency | Opisthorchiasis | Metabolic Syndrome | Glomerulonephritis, Membranous | Pyoderma Gangrenosum | Antisocial Personality Disorder | Hereditary Hemorrhagic Telangiectasia | H Syndrome | Werner's Syndrome | Hyperphosphatasia With Intellectual Disability Syndrome 4 | C3 Glomerulopathy | Goiter, Nodular | Familial Hyperaldosteronism | C3 Glomerulonephritis | Spinal Cord Diseases | Raynaud Phenomenon | Agammaglobulinemia | Cancer, Colon | Ollier Disease | Autoimmune Polyendocrinopathy Syndrome Type I | Tinea Versicolor | Thyroid Dyshormonogenesis | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Craniometaphyseal Dysplasia | Noonan Syndrome | Sickle Cell Anemia | Varicocele | Lattice Corneal Dystrophy | Hyperparathyroidism, Secondary | Angiosarcoma Of The Breast | Hypokalemia | Cystitis, Interstitial | Pulmonary Stenosis | Eccrine Porocarcinoma | Central Pain Syndrome | Prader-Willi Syndrome | Cerebrovascular Disorders | Bone Giant Cell Tumor | Interstitial Lung Diseases | Cervicitis | Gaucher Disease | Dermatitis Herpetiformis | Hyperuricemic Nephropathy, Familial Juvenile | Hypogonadism | Central Core Disease | Thyroiditis | Spinal Muscular Atrophy Type 2 | Esophageal Carcinoma | Chondroma | Diabetic Macular Edema | Seasonal Mood Disorder | Usher Syndrome Type III | Kohlschutter-Tonz Syndrome | Small Lymphocytic Lymphoma | Trichomegaly | Myocardial Infarction | Tremor | Shprintzen-Goldberg Syndrome | Cerebral Cavernous Malformations | Rickets | Schamberg Disease | Rhizomelic Chondrodysplasia Punctata | Glycogen Storage Disease Type 0, Muscle | Thyroid Hormone Resistance | Asthma | Melanoma, Malignant | Pituitary Stalk Interruption Syndrome | Fibrodysplasia Ossificans Progressiva | 3-methylglutaconic Aciduria | IMAGe Syndrome | Hodgkin Lymphoma | Infertility | Platelet Disorders | Porphyria, Acute Intermittent | Adenomyosis | Seminoma | Desbuquois Syndrome | Eczema | Krabbe Disease | Glucagonoma | Scleritis | Charcot-Marie-Tooth Disease Type 2D | Esophageal Motility Disorders | Babesiosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Lymphoma, Follicular | Multifocal Motor Neuropathy | Urea Cycle Disorder | Lymphoma | Methemoglobinemia Type IV | Myasthenia Gravis | Fragile X Syndrome | Heterotopic Ossification | Allergic Contact Dermatitis | Zollinger-Ellison Syndrome | Loeys-Dietz Syndrome Type 4 | Moyamoya Disease | Meningococcal Infections | Herpes Simplex Dermatitis | Campomelic Dysplasia | Neurofibroma, Plexiform | Weill-Marchesani Syndrome | Acute Lymphocytic Leukemia | Wieacker-Wolff Syndrome | Phenylketonuria II | CREST Syndrome | Intermittent Explosive Disorder | Coronary Heart Disease | Cockayne Syndrome | Nicolaides-Baraitser Syndrome | Primary Ovarian Insufficiency | Chronic Periodontitis | Demyelinating Diseases | Hyperhomocysteinemia | Mood Disorder | ACTH-independent Macronodular Adrenal Hyperplasia | Osteoporosis-pseudoglioma Syndrome | Chronic Mucocutaneous Candidiasis | Porphyria Cutanea Tarda | Keratocystic Odontogenic Tumor | Hereditary Folate Malabsorption | Eosinophilia | Erythematotelangiectatic Rosacea | Syphilis | Facioscapulohumeral Muscular Dystrophy Type 2 | Atopy | Pleurisy | Hypermetropia | Retinoschisis | Leukodystrophies | Sporadic Hemiplegic Migraine | Protein C Deficiency | Charcot-Marie-Tooth Disease Type 4E | Exostoses | Congenital Myopathy | Rosacea | Angiomyolipoma | Glaucoma, Congenital | Arthrogryposis | Ulcerative Colitis | Wiedemann-Steiner Syndrome | Lathosterolosis | Fibromuscular Dysplasia | Alazami Syndrome | Feingold Syndrome | Walker-Warburg Syndrome | Limb Girdle Muscular Dystrophy | Graft-versus-host Disease | Spastic Paraplegia Type 7 | Turner's Syndrome | Whipple's Disease | Papulopustular Rosacea | Hypertensive Nephropathy | Dyslipidemia | Evans Syndrome | Nance-Horan Syndrome | High Molecular Weight Kininogen Deficiency | Osmotic Demyelination Syndrome | Neuromuscular Disorders | Delirium | Shwachman-Bodian-Diamond Syndrome | Ischemia | Guanidinoacetate Methyltransferase Deficiency | Nemaline Myopathy 8 | Palsy, Cerebral | Fontaine Progeroid Syndrome | Glutaric Aciduria Type 2 | Withdrawal Syndrome | Gastric Atrophy | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Retinopathy, Diabetic | Thyrotoxic Periodic Paralysis | Ectrodactyly | Sickle Cell Disease | Pemphigus Vulgaris | Renal Oncocytoma | Hyperphenylalaninemia | Partington Syndrome | Kleine-Levin Syndrome | Meier-Gorlin Syndrome | Antiphospholipid Syndrome | Retinal Detachment | Macrodactyly | Nevus | Chylothorax, Congenital | Focal Segmental Glomerulosclerosis | Erdheim-Chester Disease | Stuttering | Chronic Beryllium Disease | Panniculitis | Endocarditis | Liebenberg Syndrome | Nasodigitoacoustic Syndrome | Neurocutaneous Syndromes | Narcolepsy | Mucolipidosis Type II | Leiomyoma | Amish Infantile Epilepsy Syndrome | Torticollis | Colitis, Collagenous | Hereditary Elliptocytosis | Christianson Syndrome