Disease

Micro Syndrome

About the Disease
Warburg Micro Syndrome 1, also known as warburg micro syndrome, is related to warburg micro syndrome 4 and warburg micro syndrome 3. An important gene associated with Warburg Micro Syndrome 1 is RAB3GAP1 (RAB3 GTPase Activating Protein Catalytic Subunit 1), and among its related pathways/superpathways are Metabolism of proteins and Vesicle-mediated transport. Affiliated tissues include eye, kidney and cerebellum, and related phenotypes are spasticity and high palate

Common Targets
RAB3GAP2 | UNC80 | RAB3GAP1 | POMK

疾病靶点研报
Micro Syndrome

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

Other Diseases

Cryptorchidism | Bullous Pemphigoid | Van Der Knaap Disease | Cherubism | Anterior Segment Dysgenesis | Xeroderma Pigmentosum | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Sezary Syndrome | Dyslipidemia | Cardiomyopathy, Dilated, 1L | Tricho-hepato-enteric Syndrome | Multiple Sclerosis | Meningococcal Meningitis | Multiple System Atrophy | Neurocysticercosis | Open-angle Glaucoma | Crohn's Disease | Borjeson-Forssman-Lehmann Syndrome | Hydrops Fetalis | Nutrition Disorders | 3-M Syndrome | Epidermolysis Bullosa Simplex | Carcinoma, Signet Ring Cell | Acute Generalized Exanthematous Pustulosis | Primary Hyperoxaluria Type 1 | Porphyria Cutanea Tarda | Retinal Vasculitis | Lassa Fever | Kohlschutter-Tonz Syndrome | Martsolf Syndrome | Mitochondrial Cytopathy | Glaucoma, Congenital | Lipodystrophy | McLeod Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Twin-to-twin Transfusion Syndrome | Jaundice, Obstructive | Alpers Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Pituitary Stalk Interruption Syndrome | Von Willebrand Disease | Oculocutaneous Albinism | Miyoshi Myopathy | Polycythemia | Niemann-Pick Disease, Type C | Basal Cell Nevus Syndrome | Succinic Semialdehyde Dehydrogenase Deficiency | Milk Allergy | Heart Septal Defects | Eccrine Porocarcinoma | Triphalangeal Thumb-polysyndactyly Syndrome | Lathosterolosis | Microphthalmia, Syndromic 7 | Lymphangiomatosis | Eiken Syndrome | Geleophysic Dysplasia | Gray Platelet Syndrome | Retinopathy, Diabetic | Cancer, Brain | Carbohydrate Metabolism Disorders | Leukocyte Adhesion Deficiency Type 1 | Urticaria | Leukodystrophies | Juvenile Myoclonic Epilepsy | Esthesioneuroblastoma | Charcot-Marie-Tooth Disease Type 4B1 | Keratoconjunctivitis | Atopy | Ichthyosis Hystrix, Curth-Macklin Type | Malignant Peripheral Nerve Sheath Tumor | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Aldosterone Synthase Deficiency | Gallstones | Wiskott-Aldrich Syndrome | Cockayne Syndrome | Mohr-Tranebjaerg Syndrome | Hereditary Spastic Paraplegia | Jalili Syndrome | Subacute Sclerosing Panencephalitis | Lichen Sclerosus | Bartter Syndrome | Trichotillomania | CREST Syndrome | Granuloma Annulare | Tinea | Guillain-Barre Syndrome | Pancytopenia | Keratosis | Vascular Calcification | Leishmaniasis, Visceral | Adenomatoid Tumor | Prader-Willi Syndrome | D-2-Hydroxyglutaric Aciduria | Thin Basement Membrane Disease | Gerodermia Osteodysplastica | Tremor | Bacterial Meningitis | Syncope | Myelodysplasia | Pulmonary Alveolar Microlithiasis | Endometrial Hyperplasia | Hypophosphatasia | Demyelinating Diseases | Keratocystic Odontogenic Tumor | Dupuytren Disease | Carcinoma, Small Cell | Urethritis | Schamberg Disease | Carotid Artery Disease | Fraser Syndrome | C3 Glomerulopathy | Osteopetrosis | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Pneumonia, Viral | Hereditary Mixed Polyposis Syndrome | Pyruvate Kinase Deficiency | Congenital Central Hypoventilation Syndrome | Malignant Fibrous Histiocytoma | Shwachman-Bodian-Diamond Syndrome | Craniofrontonasal Syndrome | Diabetic Neuropathy | Chiari Malformation Type I | Primary Ovarian Insufficiency | Sclerocornea | Coronary Heart Disease | Blomstrand Osteochondrodysplasia | Gastritis | Charcot-Marie-Tooth Disease, Type 2C | Hernia, Inguinal | Charcot-Marie-Tooth Disease Type 4 | Cramp Fasciculation Syndrome | Nevus | Anovulation | Pseudoexfoliation Syndrome | Liver Failure | Sarcoidosis | Myoclonus-dystonia Syndrome | Hyperandrogenemia | Cataract | Gastroenteritis | Bare Lymphocyte Syndrome | Pierre Robin Syndrome | Bulimia Nervosa | Primary Biliary Cholangitis | Skin Fragility-woolly Hair Syndrome | Kearns-Sayre Syndrome | Chondroma | Small Lymphocytic Lymphoma | Sulfite Oxidase Deficiency | Facioscapulohumeral Muscular Dystrophy | Biotinidase Deficiency | Giant Axonal Neuropathy | Conjunctivitis | Renal Dysplasia | Torticollis | Hepatic Adenomatosis | Empyema | Spinocerebellar Ataxia Type 28 | Huntington's Disease | Neuromuscular Disorders | Retinoschisis | Cornelia De Lange Syndrome | Nail-Patella Syndrome | Birk-Barel Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Multifocal Motor Neuropathy | Acute Lung Injury | Tumoral Calcinosis | Noonan Syndrome | Jacobsen Syndrome | Autonomic Nervous System Disorders | Congenital Dyserythropoietic Anemia Type 4 | Osteonecrosis | Dementia | Hereditary Xerocytosis | Hydrocephalus, Normal Pressure | Spinocerebellar Ataxia Type 13 | Clouston Hidrotic Ectodermal Dysplasia | Diabetes Insipidus, Nephrogenic | Beare-Stevenson Syndrome | Smoldering Myeloma | Cyst | Tietze Syndrome | Gilbert Syndrome | Schizophrenia, Paranoid | Hypercholesterolemia, Familial | Autosomal Recessive Spastic Paraplegia Type 35 | Delayed Sleep Phase Syndrome | Congenital Lipoid Adrenal Hyperplasia | Pontocerebellar Hypoplasia | Fucosidosis | Infantile Nephropathic Cystinosis | Sialoadenitis | Hemangioendothelioma | Vitamin K Deficiency | Spinocerebellar Ataxia Type 14 | Crisponi Syndrome | Tibial Muscular Dystrophy | Supravalvular Aortic Stenosis | Glaucomatocyclitic Crisis | Hereditary Pyropoikilocytosis | DOCK8 Immunodeficiency Syndrome | Blastomycosis | Schizotypal Personality Disorder | Myelomeningocele | Dengue Hemorrhagic Fever | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Pineoblastoma | Gastric Atrophy | Waldenstrom Macroglobulinemia | Thyroiditis, Autoimmune | Vascular Cognitive Impairment | Waardenburg Syndrome Type 2A | Porphyria | Melanocytic Nevus | HIBCH Deficiency | Atrial Septal Defect | Extramammary Paget's Disease | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Fetal Akinesia Deformation Sequence | Desbuquois Syndrome | Feingold Syndrome | Arts Syndrome | Central Pain Syndrome | Johanson-Blizzard Syndrome | Diffuse Palmoplantar Keratoderma | X-linked Acrogigantism | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Lymphoma Lymphoblastic | Chanarin-Dorfman Syndrome | Renal-hepatic-pancreatic Dysplasia | Spastic Paraplegia Type 7 | Hyperprolactinemia | Pupil Disorders | Keratoconus | Norrie Disease | Neurocutaneous Melanocytosis | Learning Disability | Craniopharyngioma | Familial Cerebral Amyloid Angiopathy | Sclerosteosis | Fascioliasis | Dominant Optic Atrophy | Bone Marrow Necrosis | Fahr Disease | Cocaine-Related Disorders | Congenital Afibrinogenemia | Intestinal Tuberculosis | Lattice Corneal Dystrophy | Chromosome 5q Deletion Syndrome | Stickler Syndrome | Early Infantile Epileptic Encephalopathy 13 | Blepharospasm | Pyelonephritis | Thrombocytopenia | Hyperkalemic Periodic Paralysis | Follicular Dendritic Cell Sarcoma | Uremic Pruritus | Pearson Syndrome | Exfoliative Dermatitis | Absence Epilepsy | Lymphoma, B-cell | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Dystonia Musculorum Deformans | Carney Triad | Choriocarcinoma | Enhanced S-cone Syndrome | Hypoplastic Left Heart Syndrome | Multiple Hamartoma Syndrome | DEND Syndrome | Hyperkeratosis | Intestinal Obstruction | Leukemia-lymphoma, Adult T-cell | Keloid | Pseudohypoparathyroidism Type 2 | Keratosis, Actinic | Farber Disease | Klippel-Feil Syndrome | Macular Degeneration | Sengers Syndrome | Leiomyosarcoma | Enlarged Vestibular Aqueduct | Sotos Syndrome | Amblyopia | Lattice Corneal Dystrophy Type 1 | Spondylo-ocular Syndrome | Anxiety Disorders | Carcinoid Tumor | Orthostatic Intolerance | Cerebral Amyloid Angiopathy | Keratitis-ichthyosis-deafness Syndrome | Thrombophilia | Spinocerebellar Ataxia Type 42 | Cartilage Disorders | Colon Adenoma | Pseudohypoparathyroidism Type 1B | Thrombosis | Tylosis With Esophageal Cancer | Antisynthetase Syndrome | Multiple Sulfatase Deficiency | Oligoastrocytoma | Dwarfism | Hyperammonemia | Nicotine Addiction | Cysticercosis | Paternal Uniparental Disomy Of Chromosome 14 | Acromegaly | Restless Legs Syndrome | Pre-eclampsia | Parkinson's Disease | Progressive Osseous Heteroplasia | Dystonia-parkinsonism, X-linked | Adenoma, Pituitary | Deafness, Dystonia, And Cerebral Hypomyelination | Homocystinuria | Primary Hyperoxaluria Type 3 | Trismus-pseudocamptodactyly Syndrome | Rubeosis Iridis | Thanatophoric Dysplasia | Gastroenteritis, Eosinophilic | Takayasu's Arteritis | Noonan Syndrome-like Disorder With Loose Anagen Hair | Myositis, Focal | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Glycogen Storage Disease Type 5 | Keratopathy | L-2-Hydroxyglutaric Aciduria | Urolithiasis | Chordoid Glioma | Myeloid Leukemia | Arthritis, Reactive | Vertebrobasilar Insufficiency | Adenylosuccinate Lyase Deficiency | Hypohidrotic Ectodermal Dysplasia, X-linked | Wieacker-Wolff Syndrome | Autism | Osteochondrosis | Best Macular Dystrophy | Migraine | Cabezas Syndrome | Trigonocephaly | NGLY1 Deficiency | Short-chain Acyl-CoA Dehydrogenase Deficiency | Nicolaides-Baraitser Syndrome | Danon Disease | Kabuki Syndrome 2 | Raine Syndrome | Hemochromatosis | Neurofibroma, Plexiform | Rosacea | Acute Tubular Necrosis | Nanophthalmos | Fatty Aldehyde Dehydrogenase Deficiency | Primary Lateral Sclerosis | Malnutrition | Schnyder Crystalline Corneal Dystrophy | Jawad Syndrome | Pheochromocytoma | Otopalatodigital Syndrome Type 2 | Nicotine Dependence | Carcinoma, Merkel Cell | Cannabis Abuse | Hyperglycemia | Corneal Dystrophy And Perceptive Deafness | Pernicious Anemia | Neurocutaneous Syndromes | Multiple Epiphyseal Dysplasia | Kaposiform Hemangioendothelioma | Depression | Adenosine Deaminase 2 Deficiency | Charcot-Marie-Tooth Disease Axonal Type 2N | Hereditary Hemorrhagic Telangiectasia | Congenital Aniridia | Rubinstein-Taybi Syndrome | Pontocerebellar Hypoplasia Type 2 | Myhre Syndrome | Nemaline Myopathy 8 | Cancer, Kidney | Heavy Chain Disease | Gardner Syndrome | Hypocalcemia | Trichuriasis | Persistent Fetal Circulation | Peroxisomal Disorder | Aneurysm, Thoracic Aortic | Ehlers-Danlos Syndrome | Usher Syndrome Type I | Cholera | Blepharophimosis Syndrome | Fundus Albipunctatus | Seborrheic Dermatitis | Systemic Lupus Erythematosus | Congenital Nystagmus | Walker-Warburg Syndrome | Pericarditis | C3 Glomerulonephritis | Craniolenticulosutural Dysplasia | Pulmonary Tuberculosis | Seasonal Mood Disorder | Adenocarcinoma