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.tech.

Other Diseases

Intestinal Tuberculosis | Craniofacial Dysostosis | HUPRA Syndrome | Reflex Epilepsy | Benign Familial Infantile Seizures | Ganglioneuroma | Priapism | Megalencephaly | Progressive Familial Intrahepatic Cholestasis Type 2 | Porokeratosis | Blepharospasm | Bloom Syndrome | Varicocele | Pompe Disease | Keloid | Methylmalonic Acidemia | Osteoglophonic Dysplasia | Prostatitis | Borjeson-Forssman-Lehmann Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Persistent Mullerian Duct Syndrome | Sensorineural Hearing Loss | Lattice Corneal Dystrophy | Sleep Apnea, Obstructive | Kabuki Syndrome | Gitelman Syndrome | Impetigo | Motion Sickness | Absence Epilepsy | Hepatic Steatosis | Intellectual Disability, Autosomal Dominant 5 | Vitamin B12 Deficiency | Dementia, Vascular | 3C Syndrome | Dystrophy, Cone-rod | Schizoaffective Disorder | Cholesteryl Ester Storage Disease | Language Disorders | Pleurisy | Renal Hypouricemia | Pulverulent Zonular Cataract | Cousin Syndrome | Infectious Diarrhea | Tatton-Brown-Rahman Syndrome | Bronchitis, Chronic | Diabetic Neuropathy | Birk-Barel Syndrome | Harlequin Ichthyosis | Brachial Plexus Neuropathy | Glaucomatocyclitic Crisis | Primary Hyperoxaluria | Epidermolytic Hyperkeratosis | McCune-Albright Syndrome | Alveolar Capillary Dysplasia | Esophageal Adenocarcinoma | Parvovirus B19 Infection | Anemia | Urea Cycle Disorder | Uremia | Beckwith-Wiedemann Syndrome | Paraplegia | Globozoospermia | Inborn Errors Of Metabolism | Cerebellar Ataxia, Cayman Type | Trichothiodystrophy | Granular Corneal Dystrophy | Rheumatoid Arthritis | Pontocerebellar Hypoplasia | X-linked Sideroblastic Anemia | Carey-Fineman-Ziter Syndrome | Schwannoma | Leigh Syndrome | Osmotic Demyelination Syndrome | Atopy | Poirier-Bienvenu Neurodevelopmental Syndrome | Lymphangiomatosis | Peritonitis | Adenoma, Villous | Chromosome 17q21.31 Deletion Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Hermansky-Pudlak Syndrome | Corneal Edema | Patent Foramen Ovale | Dengue Hemorrhagic Fever | Riboflavin Transporter Deficiency Neuronopathy | Diabetes Insipidus, Nephrogenic | Anosmia, Congenital | Pyruvate Carboxylase Deficiency Disease | McKusick Type Metaphyseal Chondrodysplasia | IMAGe Syndrome | Angina Pectoris | Apraxia | Spinocerebellar Ataxia Type 2 | Sarcomatoid Carcinoma Of The Lung | Renal Dysplasia | Follicular Dendritic Cell Sarcoma | Primary Cutaneous Amyloidosis | Hepatitis E | Neurofibromatosis Type 1 | Chronic Idiopathic Myelofibrosis | Multicystic Renal Dysplasia | Chloridorrhea, Congenital | Angioedema, Acquired | Nicotine Addiction | Sick Sinus Syndrome | Cataract | Desbuquois Syndrome | Spinocerebellar Ataxia Type 16 | Spinocerebellar Ataxia Type 27 | Splenomegaly | Paroxysmal Kinesigenic Dyskinesia | Spinocerebellar Ataxia | Cushing Syndrome | Leukemia-lymphoma, Adult T-cell | Endometrial Hyperplasia | Epidermolysis Bullosa Simplex | Dysthymia | Amebiasis | Charcot-Marie-Tooth Disease Type 4B1 | Liebenberg Syndrome | Cerebrovascular Disorders | Panuveitis | Hypophosphatemic Rickets, Autosomal Recessive, 1 | CDKL5 Deficiency Disorder | Dyskeratosis Congenita | Larsen Syndrome | Essential Fructosuria | Immunoproliferative Disorders | Spondylolisthesis | Focal Facial Dermal Dysplasia | Steel Syndrome | Keratitis | Supravalvular Aortic Stenosis | Hypertension, Pulmonary | Pfeiffer Syndrome | Vitamin D Deficiency | Carpal Tunnel Syndrome | Paronychia | Loeys-Dietz Syndrome | Cutaneous Mastocytosis | Malaria, Cerebral | Avian Influenza | Systemic Lupus Erythematosus | Skin Carcinoma | Charcot-Marie-Tooth Disease, Type 2A | Craniofrontonasal Syndrome | Familial Hemiplegic Migraine | Desmosterolosis | Acrocallosal Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Pseudohypoparathyroidism Type 1C | Dupuytren Disease | Tyrosinemia Type 1 | Influenza | Loeys-Dietz Syndrome Type 4 | Fahr Disease | Osteonecrosis Of The Jaw | Mitochondrial DNA Depletion Syndrome 13 | Pierpont Syndrome | Myelodysplasia | Cardiofaciocutaneous Syndrome | Small Lymphocytic Lymphoma | Purpura | Papilledema | Combined Pituitary Hormone Deficiency | Non-Langerhans Cell Histiocytosis | Hereditary Coproporphyria | Lysosomal Acid Lipase Deficiency | Adenylosuccinate Lyase Deficiency | Androgenic Alopecia | Postpartum Depression | Porphyria | Anti-glomerular Basement Membrane Disease | Multiple Sclerosis, Primary Progressive | Mitochondrial Cytopathy | Hypogammaglobulinemia | Platelet Disorders | Retinoblastoma | Achondrogenesis | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Fibrosarcoma | Cheilitis | Meningococcal Meningitis | Erythematotelangiectatic Rosacea | Von Hippel-Lindau Disease | Currarino Syndrome | Infantile Spasm | Brooke-Spiegler Syndrome | Peutz-Jeghers Syndrome | Hereditary Folate Malabsorption | Usher Syndrome Type IIC | Glomerulonephritis, Membranoproliferative | Early Infantile Epileptic Encephalopathy | Botulism | Primary Ovarian Insufficiency | Pelvic Inflammatory Disease | Charcot-Marie-Tooth Disease | Osteochondroma | Rhabdomyosarcoma, Alveolar | Major Depression | Progressive Familial Intrahepatic Cholestasis | Iron Overload | Meesmann Corneal Dystrophy | Alpha-1 Antitrypsin Deficiency | Spinocerebellar Ataxia Type 20 | Dermatomyositis | Cryptococcal Meningitis | Chromosome 16p11.2 Deletion Syndrome | Spinocerebellar Ataxia Type 10 | Gilbert Syndrome | Peroxisomal Disorder | HANAC Syndrome | Creatine Deficiency Syndrome Due To AGAT Deficiency | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Cancer, Skin | Light Chain Amyloidosis | Dentinogenesis Imperfecta | Sponastrime Dysplasia | Vici Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Rhabdomyosarcoma | Lipodystrophy | Retinal Dystrophy, Early-onset Severe | Amyotrophic Lateral Sclerosis, Juvenile | Bicuspid Aortic Valve | Mucolipidosis | Gnathodiaphyseal Dysplasia | Acute Chest Syndrome | Martsolf Syndrome | Melanoma, Malignant | Camurati-Engelmann Disease | Neural Tube Defect | Wolman Disease | Otitis Externa | Double Outlet Right Ventricle | Goiter, Nodular | Pancreatitis, Chronic | Achromatopsia | Rhabdomyosarcoma, Embryonal | Adenosine Deaminase Deficiency | Tibial Muscular Dystrophy | Waardenburg Syndrome Type 4A | Osteogenesis Imperfecta | Lissencephaly 2 | Autoimmune Polyendocrine Syndrome | Pulmonary Alveolar Microlithiasis | Rubeosis Iridis | Polyradiculopathy | Polycystic Kidney, Autosomal Dominant | McLeod Syndrome | Adenoma, Pleomorphic | TARP Syndrome | Discoid Lupus Erythematosus | Biotinidase Deficiency | Waardenburg Syndrome Type 2E | Autoimmune Autonomic Ganglionopathy | Angiodysplasia | Prune Belly Syndrome | Anterior Segment Dysgenesis | Primary Hyperoxaluria Type 3 | Hereditary Xerocytosis | Congenital Bilateral Absence Of Vas Deferens | 3-methylglutaconic Aciduria Type IV | Seizures-scoliosis-macrocephaly Syndrome | Pneumonia, Viral | Long QT Syndrome Type 1 | Protein S Deficiency | Agranulocytosis | Hypersensitivity | Thrombotic Microangiopathy | Coffin-Siris Syndrome | Polyarteritis Nodosa | Ameloblastoma | Schindler Disease | Primary Pigmented Nodular Adrenocortical Disease | Hypercalcemia | Lymphoma, Mantle Cell | Dysgerminoma | Molybdenum Cofactor Deficiency | Pancytopenia | Hypertension, Renovascular | Hyperinsulinemia | Intermittent Claudication | Myopathy | Cancer, Bladder | Pyoderma Gangrenosum | Juvenile Myelomonocytic Leukemia | Carcinoma In Situ | Episodic Ataxia Type 2 | Glioma | Hypoplastic Left Heart Syndrome | Sclerosteosis 2 | Macular Corneal Dystrophy | Diabetic Nephropathy | Progressive Osseous Heteroplasia | Spinal Muscular Atrophy Type 2 | Castleman Disease | Chronic Enteropathy Associated With SLCO2A1 Gene | Amish Infantile Epilepsy Syndrome | Familial Hyperaldosteronism | Esophagitis, Eosinophilic | Antiphospholipid Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Hypereosinophilic Syndrome | Hepatitis, Chronic | Lewy Body Dementia | Fanconi Anemia | Arthritis | Transcobalamin Deficiency | Epidermolysis Bullosa Simplex, Generalized | Cancer, Prostate | Hairy Cell Leukemia | Gastroschisis | Schwartz-Jampel-Aberfeld Syndrome | Sialidosis | Maple Syrup Urine Disease | Schnyder Crystalline Corneal Dystrophy | Fetal Alcohol Syndrome | Sorsby Fundus Dystrophy | Pneumococcal Meningitis | Seminoma | Oculopharyngeal Muscular Dystrophy | Neurodermatitis | Renal Tubular Dysgenesis | Encephalitis, Tick-borne | Tylosis With Esophageal Cancer | Depression | Imerslund-Grasbeck Syndrome | Myelitis, Transverse | Toxoplasmosis | Lipid Metabolism Disorders | Non-Hodgkin Lymphoma | Paternal Uniparental Disomy Of Chromosome 14 | Superficial Spreading Melanoma | Amelanotic Melanoma | Peripheral T-cell Lymphoma | Hypolipoproteinemia | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Pancreatitis | Methemoglobinemia | Glycogen Storage Disease Type 1 | Hypokalemic Periodic Paralysis | Tumoral Calcinosis | Craniopharyngioma | Orthostatic Intolerance | Dysfibrinogenemia | Gangliosidosis | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Familial Partial Lipodystrophy | Mitochondrial Myopathy | Hepatitis D | Twin-to-twin Transfusion Syndrome | Microtia | Hemochromatosis | Subacute Sclerosing Panencephalitis | Proopiomelanocortin Deficiency | Poikiloderma With Neutropenia | Tyrosinemia Type 2 | Basal Ganglia Cerebrovascular Disease | Panniculitis | Cutis Laxa | Bursitis | Conjunctivitis | Bardet-Biedl Syndrome | Congenital Aniridia | Familial Glucocorticoid Deficiency | Idiopathic Multicentric Castleman Disease | X-linked Acrogigantism | Intracranial Hypertension | Malonyl-CoA Decarboxylase Deficiency | Odonto-onycho-dermal Dysplasia | Melanoma, Uveal | Erectile Dysfunction | Trachoma | Chordoma | Hypotrichosis | Bietti Crystalline Dystrophy | Early Infantile Epileptic Encephalopathy 4 | Metabolic Diseases | Bartter Syndrome | Epilepsy Of Infancy With Migrating Focal Seizures | Hereditary Neuropathy With Liability To Pressure Palsies | DOCK8 Immunodeficiency Syndrome | Tularemia | Prolidase Deficiency | Nanophthalmos | Lung Diseases | Neuropathy | Enterocolitis, Necrotizing | Smith-Magenis Syndrome | Heart Block | Pseudohypoparathyroidism Type 2 | Angioedema | Ectodermal Dysplasia | Hypoparathyroidism | Bone Giant Cell Tumor | Osteoporosis, Postmenopausal | Usher Syndrome Type I | Adenomatoid Tumor | Spinocerebellar Ataxia Type 21