Disease

Stiff-man Syndrome

About the Disease
Stiff-Person Syndrome, also known as stiff-man syndrome, is related to hyperekplexia 1 and conversion disorder, and has symptoms including fever, muscle rigidity and opisthotonus. An important gene associated with Stiff-Person Syndrome is AMPH (Amphiphysin), and among its related pathways/superpathways are Neuroscience and Glucose / Energy Metabolism. The drugs Prednisone and Cytarabine have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, brain and bone, and related phenotypes are hyperhidrosis and anxiety

Common Targets
IL2

疾病靶点研报
Stiff-man Syndrome

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

Other Diseases

Malignant Peripheral Nerve Sheath Tumor | Paronychia | Arthritis, Gouty | Neurofibromatosis-Noonan Syndrome | Waardenburg Syndrome Type 1 | Renal Medullary Carcinoma | Porphyria, Acute Intermittent | NDH Syndrome | Fuchs Heterochromic Iridocyclitis | Bladder Exstrophy | Interstitial Lung Diseases | Aplastic Anemia | Aplasia Cutis Congenita | Pycnodysostosis | Pouchitis | Progressive Encephalopathy-optic Atrophy Syndrome | Cyst | Glycogen Storage Disease Type 3 | Triphalangeal Thumb-polysyndactyly Syndrome | Basan Syndrome | Primary Aldosteronism | Nephrosclerosis | Cancer, Colon | B-cell Chronic Lymphocytic Leukemia | Pneumonia, Viral | Lymphoma, Follicular | VEXAS Syndrome | Lymphangioma | Episodic Ataxia | Chordoid Glioma | Bacterial Meningitis | Raine Syndrome | Hypoalbuminemia | Aphasia | Mohr-Tranebjaerg Syndrome | Dwarfism | Glioblastoma | Benign Hereditary Chorea | Wagner Disease | Lamellar Ichthyosis | Corticobasal Syndrome | Congenital Muscular Dystrophy | Androgen Insensitivity | Diabetes Type 1 | Adenylosuccinate Lyase Deficiency | Leukoencephalopathy, Progressive Multifocal | Hemoglobinopathies | Neuropathy | Cryptosporidiosis | Sitosterolemia | Dystonia-parkinsonism, X-linked | Tardive Dyskinesia | Sorsby Fundus Dystrophy | Asperger Syndrome | Hyperparathyroidism, Primary | Ganglioneuroma | Meconium Ileus | Precocious Puberty | Hypercalcemia | Teratozoospermia | Barakat Syndrome | Obesity | Paraplegia | Desmosterolosis | Maternally Inherited Diabetes And Deafness | Phenylketonuria II | Renal Hypomagnesemia 3 | Hepatitis E | Mevalonate Kinase Deficiency | Congenital Tufting Enteropathy | Azoospermia | Plasmacytoma | Seborrheic Dermatitis | Micropenis | Hyperlipidemia | Inflammatory Myopathy | Dementia, Vascular | Neutrophilia | LRBA Deficiency | Megalencephaly | Cervicitis | Agammaglobulinemia | Cri-du-chat Syndrome | Melanocytic Nevus | Infectious Diarrhea | Duodenal Atresia | Giant Cell Glioblastoma | Subcortical Band Heterotopia | Poikiloderma With Neutropenia | Ventricular Septal Defect | Fatty Aldehyde Dehydrogenase Deficiency | Atrial Septal Defect | Scabies | Majeed Syndrome | Atherosclerosis | Cryoglobulinemia | Benign Recurrent Intrahepatic Cholestasis 1 | Hypogammaglobulinemia | Poretti-Boltshauser Syndrome | Viral Meningitis | Branchiootorenal Syndrome | Basal Ganglia Disease, Biotin-responsive | Rosacea | Rubeosis Iridis | Osteopetrosis | Sweet Syndrome | Hyperammonemia | Ectopia Lentis, Isolated, Autosomal Recessive | Syphilis | T-cell Leukemia | Paraganglioma | Peritonitis | WAGR Syndrome | Hereditary Multiple Exostoses | Giant Cell Arteritis | Fascioliasis | Wolman Disease | Congenital Poikiloderma | Wolfram Syndrome 2 | Venous Insufficiency | Prolidase Deficiency | Esophageal Adenocarcinoma | Prolactinoma | Familial Hypobetalipoproteinemia | Splenomegaly | Renal-hepatic-pancreatic Dysplasia | Strabismus | HELLP Syndrome | Scleritis | Neurocysticercosis | Pyruvate Decarboxylase Deficiency | Tangier Disease | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Cerebellar Ataxia, Cayman Type | Palsy, Cerebral | Sleep Apnea, Obstructive | Schnyder Crystalline Corneal Dystrophy | Gastrointestinal Disorders | Erythema Multiforme | Acromegaly | Pupil Disorders | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Trachoma | Frontotemporal Dementia | Neural Tube Defect | Choroideremia | Pityriasis Rubra Pilaris | Nephrotic Syndrome | Hyperprolactinemia | Hypogonadism | Erythema Nodosum | Schamberg Disease | Alzheimer Disease, Late Onset | Uremia | Hypotrichosis Simplex | Hepatitis D | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Chronic Thromboembolic Pulmonary Hypertension | Polyomavirus Nephropathy | Congenital Generalized Lipodystrophy | Kleine-Levin Syndrome | Stroke, Hemorrhagic | Corneal Dystrophy And Perceptive Deafness | Keratitis-ichthyosis-deafness Syndrome | Fibrosarcoma | Pontocerebellar Hypoplasia Type 2 | Castleman Disease | Spinocerebellar Ataxia Type 38 | Wolfram Syndrome | Cat Eye Syndrome | Enterocolitis, Necrotizing | Angelman Syndrome | Exfoliative Dermatitis | Narcolepsy | Tumoral Calcinosis | Glomerulonephritis | Greenberg Dysplasia | Macrodactyly | Empyema | Pituitary Dwarfism | Antisynthetase Syndrome | Dementia | Charcot-Marie-Tooth Disease | Otitis Media | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Vitamin B12 Deficiency | Hennekam Lymphangiectasia-lymphedema Syndrome | Albinism | Charcot-Marie-Tooth Disease, Type 2C | Hemorrhagic Disorders | Osteogenesis Imperfecta | Prolymphocytic Leukemia | Familial Retinal Arterial Macroaneurysm | Greig Cephalopolysyndactyly Syndrome | Fukuyama Congenital Muscular Dystrophy | Restrictive Dermopathy | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Riboflavin Transporter Deficiency Neuronopathy | Ollier Disease | Spinocerebellar Ataxia Type 17 | Oligoastrocytoma | 3-methylcrotonyl-CoA Carboxylase Deficiency | Neuroectodermal Tumors, Primitive | Hartnup Disease | Mosaic Variegated Aneuploidy Syndrome 2 | Spasticity | Congenital Dysfibrinogenemia | Ophthalmoplegia | Intracranial Hypertension | Acute Coronary Syndrome | Oculopharyngeal Muscular Dystrophy | Acrodysostosis | Hemangioblastoma | Cystitis | Progressive Myoclonic Epilepsy | Chordoma | Keratopathy | Multiple Myeloma | Rothmund-Thomson Syndrome | Zimmermann-Laband Syndrome | Cerebral Cavernous Malformations | Irritable Bowel Syndrome | Blue Nevus | Pyruvate Dehydrogenase Deficiency | Retinal Detachment | Ectrodactyly | Osteogenesis Imperfecta Type VI | Congenital Disorders Of Glycosylation Type II | Wolcott-Rallison Syndrome | Encephalocele | CREST Syndrome | Leishmaniasis, Cutaneous | Chylothorax, Congenital | Megaloblastic Anemia | Hypersomnia | Larsen Syndrome | Spermatocele | CHARGE Syndrome | Sialoadenitis | Fucosidosis | Graft-versus-host Disease | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Avian Influenza | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Oligospermia | Nephropathy | Toxoplasmosis | Hyperparathyroidism, Secondary | B-cell Prolymphocytic Leukemia | Communication Disorders | Glaucoma, Congenital | Beta-Propeller Protein-associated Neurodegeneration | VACTERL Association | DICER1 Syndrome | Nanophthalmos | Neurodevelopmental Disorders | Schwannomatosis | Left Ventricular Noncompaction | Glanzmann Thrombasthenia | Anemia | Carney Triad | Polymyalgia Rheumatica | Diabetes Insipidus, Nephrogenic | Microphthalmia, Syndromic 7 | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Neurofibroma, Plexiform | Crigler-Najjar Syndrome | Trichuriasis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Pfeiffer Syndrome | 5-oxoprolinase Deficiency | Charcot-Marie-Tooth Disease Type 4E | Okihiro Syndrome | Vaginitis | Johanson-Blizzard Syndrome | Neutropenia | Compartment Syndrome | Cold-induced Sweating Syndrome | Lymphopenia | Angioimmunoblastic T-cell Lymphoma | Dermatomyositis | Goiter | Hemophilia | Otopalatodigital Syndrome Type 2 | Cholestasis | Lysosomal Acid Lipase Deficiency | Oculocutaneous Albinism | Echinococcosis | Hepatopulmonary Syndrome | Persistent Mullerian Duct Syndrome | Osteochondrosis | Myopia | Lateral Meningocele Syndrome | Saethre-Chotzen Syndrome | Bare Lymphocyte Syndrome | Tenosynovial Giant Cell Tumor | Cholangiocarcinoma | Myotonia | Amebiasis | Spinocerebellar Ataxia Type 1 | Hypertension | Distal Spinal Muscular Atrophy | Blepharoconjunctivitis | Galactosialidosis | Schwartz-Jampel-Aberfeld Syndrome | Creutzfeldt-Jakob Disease | Gigantism | Epidermolysis Bullosa | Diarrhea | Chromosome 5q Deletion Syndrome | Light Chain Amyloidosis | Huntington's Disease-like 2 | Methemoglobinemia | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Hemochromatosis Type 1 | Spinocerebellar Ataxia Type 7 | Spinocerebellar Ataxia Type 27 | Lafora Disease | Thyroid Dysgenesis | Marshall-Smith Syndrome | Osteoporosis | Isovaleric Acidemia | Antenatal Bartter Syndrome Type 1 | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Hepatorenal Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Intellectual Disability, Autosomal Dominant 5 | Adrenal Insufficiency | Spinocerebellar Ataxia Type 28 | Conjunctivitis, Allergic | Achondrogenesis | Hermansky-Pudlak Syndrome | Bietti Crystalline Dystrophy | Angioedema, Hereditary | Pure Autonomic Failure | Infantile Nephropathic Cystinosis | Aicardi-Goutieres Syndrome | Acute Myeloid Leukemia | Anovulation | Sarcoma | Schizencephaly | Autosomal Recessive Spastic Paraplegia Type 54 | Fibronectin Glomerulopathy | Pseudo-pseudohypoparathyroidism | Cornelia De Lange Syndrome | Spinocerebellar Ataxia Type 21 | Congenital Diaphragmatic Hernia | Carcinoma, Small Cell | Cocaine-Related Disorders | Colon Adenoma | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Binge Eating Disorder | Thrombophlebitis | Citrullinemia | Endocarditis | Hartsfield Syndrome | Arthritis, Reactive | Reflex Epilepsy | Headache | Actinomycetoma | Unverricht-Lundborg Syndrome | Osteogenesis Imperfecta Type V | Primary Lateral Sclerosis | CDKL5 Deficiency Disorder | Cystinosis | Trichothiodystrophy | Familial Hemiplegic Migraine | Glucagonoma | Endometrial Hyperplasia | Ectodermal Dysplasia | Lesch-Nyhan Syndrome | Aldosterone Deficiency | Mountain Sickness | Guillain-Barre Syndrome | Rolandic Epilepsy | Asphyxia Neonatorum | Williams Syndrome | Alazami Syndrome | Spinocerebellar Ataxia Type 8 | Epidermolysis Bullosa Simplex, Localized | Mitochondrial DNA Depletion Syndrome 13 | Limb Girdle Muscular Dystrophy | 3-M Syndrome | Vascular Cognitive Impairment | Cohen Syndrome | Hereditary Inclusion Body Myopathy | Pemphigoid | Panniculitis | Shock, Cardiogenic | Urofacial Syndrome | Cantu Syndrome | Sclerocornea | Skin Carcinoma | Fanconi Syndrome | Urolithiasis | Osmotic Demyelination Syndrome | Epithelioid Hemangioma | Pneumococcal Meningitis | Polycystic Kidney, Autosomal Dominant