Chudley-McCullough Syndrome

About the Disease
Chudley-Mccullough Syndrome, also known as deafness, sensorineural, with partial agenesis of the corpus callosum and arachnoid cysts, is related to arachnoid cysts, intracranial and sensorineural hearing loss. An important gene associated with Chudley-Mccullough Syndrome is GPSM2 (G Protein Signaling Modulator 2). Affiliated tissues include brain, pituitary and bone marrow, and related phenotypes are hydrocephalus and intellectual disability, mild

Common Targets
GPSM2

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

Other Diseases

Autoimmune Polyendocrine Syndrome | GATA2 Deficiency | Multicentric Carpotarsal Osteolysis Syndrome | Mabry Syndrome | Methemoglobinemia | Angelman Syndrome | H Syndrome | Congenital Fiber-type Disproportion Myopathy | Anovulation | Cenani-Lenz Syndactyly Syndrome | Knobloch Syndrome | Sarcoma, Alveolar Soft Part | Leprosy | Retinal Dystrophy, Early-onset Severe | Okihiro Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Acral Lentiginous Melanoma | Acrodysostosis | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | MIRAGE Syndrome | Hypopigmentation | Multiple Sclerosis, Primary Progressive | Retinoblastoma | Walker-Warburg Syndrome | Bloom Syndrome | Osteogenesis Imperfecta Type IV | Metatropic Dysplasia | Familial Mediterranean Fever | Rubinstein-Taybi Syndrome | Cardiomyopathy, Hypertrophic | Scleritis | Plasmacytoma | Demyelinating Diseases | Leber Congenital Amaurosis | Tuberculosis | Malaria, Cerebral | Major Depression | Otitis Media | Epicondylitis | Genee-Wiedemann Syndrome | Diabetes Mellitus, Transient Neonatal | Atopy | Abetalipoproteinemia | Dystonia-parkinsonism, X-linked | Encephalitis, Tick-borne | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Traboulsi Syndrome | Cardiac Sarcoidosis | Corneal Dystrophy | N-acetylglutamate Synthase Deficiency | Schuurs-Hoeijmakers Syndrome | Raine Syndrome | Hypersensitivity | Epidermolysis Bullosa Acquisita | Ophthalmoplegia | Myhre Syndrome | Primary Biliary Cholangitis | Carcinoma, Squamous Cell | Neurodegeneration With Brain Iron Accumulation | Depression | ADNP Syndrome | Myotonic Disorders | Takayasu's Arteritis | Analgesia | Enlarged Vestibular Aqueduct | Pseudohypoaldosteronism | Charcot-Marie-Tooth Disease Type 2D | Klippel-Feil Syndrome | Cystinuria | Globozoospermia | Glutathione Synthetase Deficiency | Pseudohypoparathyroidism Type 2 | Hemophilia | GLUT1 Deficiency Syndrome | Varices | Lysosomal Acid Lipase Deficiency | Rolandic Epilepsy | Alopecia Areata | Diabetes Insipidus | Benign Familial Pemphigus | Cohen Syndrome | Pierpont Syndrome | Donnai-Barrow Syndrome | Hepatitis, Autoimmune | Fuchs Heterochromic Iridocyclitis | Budd-Chiari Syndrome | Molybdenum Cofactor Deficiency | Renal Hypomagnesemia 3 | Kallmann Syndrome | Oligoasthenoteratozoospermia | Multiple System Atrophy | Leukoplakia, Oral | Thyroiditis, Autoimmune | Niemann-Pick Disease | Chronic Leukemia | Diffuse Mesangial Sclerosis | Cardiomyopathy, Restrictive | Inborn Errors Of Metabolism | Thrombotic Microangiopathy | Chondroma | Infertility | Interstitial Lung Diseases | Duane Retraction Syndrome | Gardner Syndrome | Idiopathic Multicentric Castleman Disease | Tetanus | Adenocarcinoma | Craniopharyngioma | Ellis-Van Creveld Syndrome | Giant Cell Glioblastoma | Pituitary Dwarfism | Alpers Syndrome | T-cell Leukemia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Rash | Atherosclerosis | Episodic Ataxia Type 1 | Pernicious Anemia | Ichthyosis | Sarcoidosis | Mevalonate Kinase Deficiency | Endocarditis | Usher Syndrome Type IIC | McLeod Syndrome | Veno-occlusive Disease | Gray Platelet Syndrome | Osteogenesis Imperfecta Type V | Skin Carcinoma | Juvenile Myelomonocytic Leukemia | Hypoproteinemia, Hypercatabolic | Mastitis | Esophageal Adenocarcinoma | Sarcoma | Acute Leukemia | Bursitis | Leber Hereditary Optic Neuropathy | Spinocerebellar Ataxia Type 40 | Lassa Fever | HELLP Syndrome | Infectious Diarrhea | Babesiosis | Hypermethioninemia | Dwarfism | Chronic Beryllium Disease | Adenosine Deaminase 2 Deficiency | Neurodevelopmental Disorders | Fibromyalgia | Common Cold | Long QT Syndrome Type 1 | Spinocerebellar Ataxia Type 15 | Spinocerebellar Ataxia Type 31 | Methylmalonic Acidemia | Acute Kidney Injury | Autoimmune Hemolytic Anemia | Scleroderma, Diffuse | Hypertension | Carey-Fineman-Ziter Syndrome | Charcot-Marie-Tooth Disease Type 3 | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Ligneous Conjunctivitis | Canavan Disease | Retinitis Pigmentosa 3 | Huntington's Disease | Birk-Barel Syndrome | Insulinoma | Acute Tubular Necrosis | Ataxia-ocular Apraxia 2 | Charcot-Marie-Tooth Disease, Type 1A | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Neurofibromatosis Type 1 | Norrie Disease | Hypertensive Retinopathy | Barakat Syndrome | Immunoproliferative Disorders | Pachyonychia Congenita | Asthma | Hyperkeratosis | Motion Sickness | Lymphoproliferative Disorders | Encephalopathy, Ethylmalonic | Rheumatoid Arthritis | Sarcosinemia | Osteosarcoma | Muir-Torre Syndrome | Mannosidase Deficiency Diseases | Keratitis-ichthyosis-deafness Syndrome | Antisocial Personality Disorder | Gastritis | Vitreoretinal Degeneration, Snowflake Type | Familial Glucocorticoid Deficiency | Myocarditis | Pemphigoid | Cancer, Colon | Spinocerebellar Ataxia | Cheilitis | Proximal Symphalangism | Diabetic Encephalopathy | Erectile Dysfunction | Adams-Oliver Syndrome | Angina Pectoris | Behavioral Variant Of Frontotemporal Dementia | Thalassemia, Beta | Carbamoyl Phosphate Synthetase I Deficiency | Hepatorenal Syndrome | Huntington's Disease-like 2 | Hypersomnia | Erythropoietic Protoporphyria | Familial Hypobetalipoproteinemia | Chiari Malformation Type I | Hypoalbuminemia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Facioscapulohumeral Muscular Dystrophy Type 2 | Retinal Degeneration | Vitamin K Deficiency | Hemimegalencephaly | Allan-Herndon-Dudley Syndrome | Exfoliative Dermatitis | Cancer, Skin | Frontometaphyseal Dysplasia | Zellweger Syndrome | Cushing Syndrome | FG Syndrome | Antiphospholipid Syndrome | Schwannomatosis | Papillon-Lefevre Syndrome | Carney-Stratakis Syndrome | Otitis Externa | Swine Influenza | Bietti Crystalline Dystrophy | Polycythemia | Arterial Tortuosity Syndrome | Hyperbilirubinemia | Early Infantile Epileptic Encephalopathy 13 | Gangliosidosis, GM1 | Primary Hyperoxaluria Type 1 | Generalized Epilepsy And Paroxysmal Dyskinesia | Gestational Trophoblastic Disease | Charcot-Marie-Tooth Disease | Shwachman-Bodian-Diamond Syndrome | Sengers Syndrome | Basal Ganglia Disease | Oculocutaneous Albinism Type 1 | Guttate Psoriasis | Hypobetalipoproteinemias | Sialidosis Type I | Seizures | Inflammatory Myofibroblastic Tumor | Small Lymphocytic Lymphoma | Antisynthetase Syndrome | Congenital Absence Of Vas Deferens | Disseminated Superficial Actinic Porokeratosis | Pantothenate Kinase-associated Neurodegeneration | Usher Syndrome Type I | Ectodermal Dysplasia | Cri-du-chat Syndrome | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Nephroblastoma | Congenital Muscular Dystrophy | Congenital Dyserythropoietic Anemia | Progressive Familial Intrahepatic Cholestasis Type 3 | Hyperuricemia | Thyroid Dyshormonogenesis | Charcot-Marie-Tooth Disease Type 2T | Trichomegaly | Spinal Muscular Atrophy Type 3 | Esophageal Carcinoma | Schamberg Disease | Hartnup Disease | Neurocutaneous Syndromes | Tracheal Disorders | Extramammary Paget's Disease | CHARGE Syndrome | Congenital Lipoid Adrenal Hyperplasia | Amenorrhea | Paraplegia | Best Macular Dystrophy | 3-M Syndrome | Autosomal Recessive Spastic Paraplegia Type 75 | WAGR Syndrome | Combined Malonic And Methylmalonic Acidemia | Acute Chest Syndrome | Epidermodysplasia Verruciformis | Epidermolysis Bullosa | Chloridorrhea, Congenital | Macrophage Activation Syndrome | Eclampsia | Cholangitis | Lymphangioleiomyomatosis | Hepatitis C, Chronic | Burn-McKeown Syndrome | Encephalitis | Wilson's Disease | Dementia | Eccrine Porocarcinoma | Myoclonic Atonic Epilepsy | Lymphedema | Herpes Genitalis | Pseudo-pseudohypoparathyroidism | Rett Syndrome | Wolcott-Rallison Syndrome | Jacobsen Syndrome | Rosacea | Periventricular Nodular Heterotopia | Hypocalcemia | Mountain Sickness | Congenital Dyserythropoietic Anemia Type 4 | B-cell Chronic Lymphocytic Leukemia | Arthrogryposis | Neuroectodermal Tumors, Primitive | Carotid Artery Disease | Fibronectin Glomerulopathy | Brachial Plexus Neuropathy | Synpolydactyly | Acute Anterior Uveitis | Corneal Dystrophy And Perceptive Deafness | Bartsocas-Papas Syndrome | Christianson Syndrome | Chromosome 9q34.3 Deletion Syndrome | Cancer, Kidney | Pilomatrix Carcinoma | Waardenburg Syndrome Type 2E | Camurati-Engelmann Disease | Neuroleptic Malignant Syndrome | Achondrogenesis | Spermatocele | Generalized Epilepsy With Febrile Seizures Plus | Chronic Neutrophilic Leukemia | Primary Progressive Nonfluent Aphasia | Bipolar Disorder | Proteasome-associated Autoinflammatory Syndrome 2 | Microphthalmia | Protein S Deficiency | Mucolipidosis Type IV | Multiple Sclerosis, Chronic Progressive | Rubeosis Iridis | Retinoschisis | Primary Familial Brain Calcification | Carcinoma, Small Cell | Glycogen Storage Disease Type 4 | Glanzmann Thrombasthenia | Congenital Nephrotic Syndrome | Peyronie's Disease | Hepatitis | Schindler Disease | Blastomycosis | 3-hydroxy-3-methylglutaric Aciduria | Oligoastrocytoma | Hyperprolactinemia | Nail Disorder, Nonsyndromic Congenital | Smith-Kingsmore Syndrome | Systemic Lupus Erythematosus | Patent Foramen Ovale | Specific Granule Deficiency | Borderline Personality Disorder | Esthesioneuroblastoma | GM2-gangliosidosis AB Variant | Gastrointestinal Disorders | Infantile Liver Failure Syndrome 1 | Pure Autonomic Failure | McKusick Type Metaphyseal Chondrodysplasia | Peripheral Neuropathy | Hypertension, Pulmonary | Lentigo | Hemolytic Uremic Syndrome, Atypical | Goiter | Phenylketonuria | Infantile Nephropathic Cystinosis | Prune Belly Syndrome | Miyoshi Myopathy | Urea Cycle Disorder | Plasma Cell Leukemia | Multifocal Motor Neuropathy | Glomerulonephritis | Allergic Contact Dermatitis | Lipoma | Chronic Idiopathic Myelofibrosis | Meningioma, Benign | Necrobiosis Lipoidica | Twin-to-twin Transfusion Syndrome | Cluster Headache | Pineoblastoma | Porphyria Cutanea Tarda | Hemochromatosis Type 1 | Ocular Surface Squamous Neoplasia | Chromosome 16p11.2 Deletion Syndrome | Chronic Thromboembolic Pulmonary Hypertension | Narcolepsy | Spondylometaphyseal Dysplasia | Hyperacusis | Cryopyrin-associated Periodic Syndromes | Exocrine Pancreatic Insufficiency | HIBCH Deficiency | Autosomal Recessive Congenital Ichthyosis | Glomerulonephritis, Membranoproliferative | Bicuspid Aortic Valve | Hepatic Adenomatosis | Purpura, Thrombotic Thrombocytopenic | Leishmaniasis, Cutaneous | Meningeal Melanocytoma | Guanidinoacetate Methyltransferase Deficiency