3C Syndrome

About the Disease
Ritscher-Schinzel Syndrome, also known as 3c syndrome, is related to ritscher-schinzel syndrome 2 and ritscher-schinzel syndrome 1. An important gene associated with Ritscher-Schinzel Syndrome is WASHC5 (WASH Complex Subunit 5). Affiliated tissues include heart.

Common Targets
WDR91 | CCDC22 | MASP1 | VPS35L

Note: If you'd like to get a target analysis report for 3C 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 3C Syndrome at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Lymphoma, Follicular | Sickle Cell Disease | Superficial Spreading Melanoma | Hepatitis B, Chronic | Hartsfield Syndrome | Giant Axonal Neuropathy | Thyroiditis | Thrombophilia | Osteochondrosis | Mitochondrial DNA Depletion Syndrome | Long QT Syndrome Type 1 | Necrotizing Autoimmune Myopathy | Diffuse Intrinsic Pontine Glioma | Melanoma | Osteomalacia | Long QT Syndrome Type 2 | Leukodystrophies | Lentigo | Pneumococcal Meningitis | Neutrophilia | Cervical Dystonia | Ovarian Hyperstimulation Syndrome | Pulmonary Tuberculosis | Optic Neuritis | Carney-Stratakis Syndrome | Stroke, Ischemic | Progressive External Ophthalmoplegia | Osteoporosis, Postmenopausal | Rhinitis | Hyperparathyroidism, Primary | Paraganglioma, Carotid Body | HELLP Syndrome | Blepharophimosis Syndrome | Sweet Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Diamond-Blackfan Anemia | Kearns-Sayre Syndrome | Osteogenesis Imperfecta Type V | Lymphedema | Spinocerebellar Ataxia Type 23 | Amelogenesis Imperfecta | Anosmia, Congenital | Osteogenesis Imperfecta | Nephrotic Syndrome | Treacher Collins Syndrome | Thrombosis | Hyperammonemia | Lateral Meningocele Syndrome | Achondrogenesis | Ischemia | Sandhoff Disease | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Hereditary Neuropathy With Liability To Pressure Palsies | Alpers Syndrome | Polycystic Liver | Gynecomastia | Bronchiolitis | Avian Influenza | Pyoderma Gangrenosum | Arrhythmogenic Right Ventricular Cardiomyopathy | Rhizomelic Chondrodysplasia Punctata | Hypohidrotic Ectodermal Dysplasia | Maple Syrup Urine Disease | Gerstmann-Straussler-Scheinker Syndrome | Acute Motor Axonal Neuropathy | Gaucher Disease | Ovarian Sex Cord-stromal Tumor | Metachondromatosis | Dyslipidemia | Benign Familial Pemphigus | Marinesco-Sjogren Syndrome | Diabetes Type 1 | Tenosynovial Giant Cell Tumor | Bernard-Soulier Syndrome | Sarcosinemia | Cushing Syndrome | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Enlarged Vestibular Aqueduct | Brenner Tumor | Ghosal Syndrome | Urethritis | Coffin-Lowry Syndrome | Lipid Metabolism Disorders | Gangliosidosis | Congenital Heart Block | Hyperuricemia | Neurocutaneous Melanocytosis | FG Syndrome | Lesch-Nyhan Syndrome | N-acetylglutamate Synthase Deficiency | Waardenburg Syndrome Type 1 | Hydrocephalus, Normal Pressure | Autosomal Recessive Bestrophinopathy | Metatropic Dysplasia | Lymphangioma | Retinopathy Of Prematurity | Craniofrontonasal Syndrome | Chordoid Glioma | Aicardi-Goutieres Syndrome | Hemolytic Uremic Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Transcobalamin Deficiency | Renal Failure | Poikiloderma With Neutropenia | Cardiomyopathy, Dilated, 1L | Glioma | Camptocormia | Adenoma, Pituitary | Porencephaly | Endocarditis | Glutaric Aciduria Type 1 | Charcot-Marie-Tooth Disease Type 4E | Familial Glucocorticoid Deficiency | Apert Syndrome | Creutzfeldt-Jakob Disease | Schuurs-Hoeijmakers Syndrome | ICF Syndrome | Filariasis | Congenital Tufting Enteropathy | Myocardial Infarction | Thanatophoric Dysplasia Type 1 | Polyradiculopathy | Bulimia Nervosa | Chronic Inflammatory Demyelinating Polyneuropathy | Mastitis | Hereditary Coproporphyria | Paronychia | Hemolytic Uremic Syndrome, Atypical | Cryptosporidiosis | Generalized Epilepsy With Febrile Seizures Plus | Ollier Disease | Hypereosinophilic Syndrome | Diabetic Nephropathy | Limb Girdle Muscular Dystrophy | Antenatal Bartter Syndrome Type 1 | Hemochromatosis | Vitiligo | Alopecia Areata | Spastic Paraplegia Type 7 | Choroiditis | Isobutyryl-CoA Dehydrogenase Deficiency | Short-chain Acyl-CoA Dehydrogenase Deficiency | Antiphospholipid Syndrome | Usher Syndrome Type IIC | Acne | Wieacker-Wolff Syndrome | CEDNIK Syndrome | Leiomyosarcoma | Cholelithiasis | Periventricular Nodular Heterotopia | Lipid Storage Myopathy | Erythema Multiforme | Gliosarcoma | Dysequilibrium Syndrome | Neuropathy | Nemaline Myopathy 10 | Early Infantile Epileptic Encephalopathy 1 | Bullous Pemphigoid | HUPRA Syndrome | Synovitis | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Colitis, Lymphocytic | Colitis, Collagenous | Tonsillitis | Acute Coronary Syndrome | Lymphoproliferative Disorders | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Central Pain Syndrome | Metabolic Diseases | Interstitial Lung Diseases | Carcinoma, Small Cell | Megalencephaly | Spinal Muscular Atrophy | Anorectal Fistula | Huntington's Disease-like 2 | Heart Failure | Intestinal Obstruction | Congenital Dysfibrinogenemia | Inflammatory Joint Disease | Optic Neuropathy, Anterior Ischemic | Sitosterolemia | Chronic Thromboembolic Pulmonary Hypertension | Osteoarthritis | Bicuspid Aortic Valve | Neurocutaneous Syndromes | Endometritis | Keratosis | Pyruvate Dehydrogenase Deficiency | Birk-Barel Syndrome | Adrenoleukodystrophy, X-linked | Infantile Refsum Disease | Hidradenitis Suppurativa | Pernicious Anemia | Nestor-Guillermo Progeria Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Pheochromocytoma | Cryptococcal Meningitis | Duodenal Atresia | Chondrodysplasia Punctata 1, X-linked Recessive | Amyotrophic Lateral Sclerosis | Spinocerebellar Ataxia Type 10 | Spinocerebellar Ataxia Type 8 | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Pendred Syndrome | Pigment Dispersion Syndrome | Rosacea | Leukemia-lymphoma, Adult T-cell | Myoclonic Epilepsy With Ragged Red Fibers | Osteogenesis Imperfecta Type II | Familial Isolated Hyperparathyroidism | Mitochondrial DNA Depletion Syndrome 13 | Lennox-Gastaut Syndrome | Sclerosteosis | Carcinoma, Merkel Cell | Hypospadias | Hypertension, Renovascular | Nephrotic Syndrome Type 1 | Paget's Disease Of The Breast | Porokeratosis | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Myasthenia Gravis | Cysticercosis | 3-methylcrotonyl-CoA Carboxylase Deficiency | Sorsby Fundus Dystrophy | Nicotine Addiction | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Hemorrhage | Papillon-Lefevre Syndrome | Metanephric Adenoma | Neuroleptic Malignant Syndrome | Epilepsy | Aspartylglycosaminuria | KBG Syndrome | Inborn Errors Of Metabolism | Non-small Cell Lung Cancer | Neuronal Ceroid Lipofuscinosis | Familial Hypertrophic Cardiomyopathy | Primary Hyperoxaluria | Lactose Intolerance | Chorioretinitis | Orotic Aciduria | Heterotopic Ossification | Kidney Stones | Chondromyxoid Fibroma | Hemorrhoids | Hereditary Inclusion Body Myopathy | Corneal Neovascularization | Hypogammaglobulinemia | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Common Cold | Lipoma | Anal Fissure | Echinococcosis | Triphalangeal Thumb-polysyndactyly Syndrome | Juvenile Hyaline Fibromatosis | Glaucoma | Osmotic Demyelination Syndrome | Neurodevelopmental Disorders | Atrial Septal Defect | Sialidosis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Spinocerebellar Ataxia Type 6 | Intestinal Hypomagnesemia 1 | Exocrine Pancreatic Insufficiency | Primary Progressive Aphasia | Poretti-Boltshauser Syndrome | Glycogen Storage Disease Type 9 | Duane Retraction Syndrome | Pseudo-pseudohypoparathyroidism | Encephalitis, Tick-borne | Schwannomatosis | 3-methylglutaconic Aciduria Type I | Avellino Corneal Dystrophy | Megaloblastic Anemia | Multisystemic Smooth Muscle Dysfunction Syndrome | Leukoplakia | Seizures-scoliosis-macrocephaly Syndrome | Constipation | Viral Meningitis | Keloid | Alpha-thalassemia Myelodysplasia Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Von Hippel-Lindau Disease | C3 Glomerulonephritis | Conn Syndrome | Arthropathy | Cystinuria | Reticular Dysgenesis | LEOPARD Syndrome | Carcinoid Syndrome | Acute Generalized Exanthematous Pustulosis | Chondrosarcoma | Hydrops Fetalis | Juvenile Myelomonocytic Leukemia | Vitamin K Deficiency | Fetal Alcohol Syndrome | Enhanced S-cone Syndrome | Zellweger Syndrome | Spinocerebellar Ataxia Type 17 | Gastritis | B-cell Prolymphocytic Leukemia | Hyperoxaluria | Stuve-Wiedemann Syndrome | Acquired Partial Lipodystrophy | Pituitary Dwarfism | Pseudohypoparathyroidism Type 1A | Polymyalgia Rheumatica | Polyneuropathy | VACTERL/VATER Association | Veno-occlusive Disease | MIRAGE Syndrome | Neurofibromatosis Type 2 | Endophthalmitis | Strabismus | Familial Hemiplegic Migraine | Sturge-Weber Syndrome | Charcot-Marie-Tooth Disease Type 3 | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Connective Tissue Disorders | Autism | Synpolydactyly | Stargardt Disease | Paternal Uniparental Disomy Of Chromosome 14 | Parapsoriasis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Blastoma, Pleuropulmonary | GAPO Syndrome | Pleural Tuberculosis | Schaaf-Yang Syndrome | Hemophilia | Rhabdomyosarcoma, Embryonal | Scabies | Vertigo | Intermittent Explosive Disorder | Double Outlet Right Ventricle | Erythematotelangiectatic Rosacea | Angiosarcoma | WAGR Syndrome | Burn-McKeown Syndrome | Dowling-Degos Disease | Mucolipidosis Type III | Plasma Cell Leukemia | Osteogenesis Imperfecta Type VI | Tendinopathy | Medulloblastoma | CHOPS Syndrome | Pupil Disorders | Retinal Degeneration | Cabezas Syndrome | Lymphedema-distichiasis Syndrome | Glutaric Aciduria Type 3 | Progressive Familial Intrahepatic Cholestasis Type 2 | Mycosis Fungoides | Castleman Disease | Spondylolisthesis | Pantothenate Kinase-associated Neurodegeneration | Depression | Macrophage Activation Syndrome | Kaposi Sarcoma | Skin Fragility-woolly Hair Syndrome | Hypermetropia | Hepatitis, Alcoholic | Infantile Liver Failure Syndrome 1 | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Optic Neuropathy | Autoimmune Polyendocrine Syndrome | Vogt-Koyanagi-Harada Syndrome | Multiple Hamartoma Syndrome | Spermatocele | Ectodermal Dysplasia | McCune-Albright Syndrome | Dengue Hemorrhagic Fever | Renal-hepatic-pancreatic Dysplasia | REM Sleep Behavior Disorder | Fukuyama Congenital Muscular Dystrophy | Warsaw Breakage Syndrome | Epiphyseal Chondrodysplasia, Miura Type | Phenylketonuria II | Eccrine Porocarcinoma | Cornelia De Lange Syndrome | Nephronophthisis | Diffuse Mesangial Sclerosis | Schistosomiasis Mansoni | Familial Mediterranean Fever | Osteitis | Basal Cell Nevus Syndrome | Muckle-Wells Syndrome | Craniometaphyseal Dysplasia | Sarcoma, Alveolar Soft Part | Intestinal Pseudo-obstruction | Idiopathic Multicentric Castleman Disease | Cancer, Prostate | Encephalocele | Charcot-Marie-Tooth Disease Type 4 | Brachial Plexus Neuropathy | Tricho-hepato-enteric Syndrome | Gastroenteritis | Barrett Esophagus | Peritonitis