Fukuyama Congenital Muscular Dystrophy

About the Disease
Muscular Dystrophy-Dystroglycanopathy , Type a, 4, also known as fukuyama congenital muscular dystrophy, is related to cdags syndrome and polymicrogyria, and has symptoms including seizures An important gene associated with Muscular Dystrophy-Dystroglycanopathy , Type a, 4 is FKTN (Fukutin), and among its related pathways/superpathways are Metabolism of proteins and Diseases of glycosylation. Affiliated tissues include eye, brain and skeletal muscle, and related phenotypes are gait disturbance and global developmental delay

Common Targets
PLD1 | POMT1 | FKTN | CENPJ | TMCO1

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

Other Diseases

Lattice Corneal Dystrophy Type 1 | Pyoderma Gangrenosum | Diabetes Insipidus, Nephrogenic | Tuberculous Meningitis | Cerebellofaciodental Syndrome | Craniopharyngioma | Treacher Collins Syndrome | Tylosis With Esophageal Cancer | Epidermolysis Bullosa Dystrophica | Cystinosis | Meleda Disease | Netherton Syndrome | Transthyretin-related Amyloidosis | Leukodystrophies | Presbycusis | Arteriovenous Malformations | Xeroderma Pigmentosum Variant Type | Neurotoxicity | Facioscapulohumeral Muscular Dystrophy Type 2 | Granular Corneal Dystrophy | Glycogen Storage Disease Type 1b | Urticaria | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Lymphoma Lymphoblastic | Encephalopathy, Glycine | Glutathione Synthetase Deficiency | Pseudohypoparathyroidism Type 1A | Tatton-Brown-Rahman Syndrome | Hypoplastic Left Heart Syndrome | Colorectal Adenoma | Uveitis | Eclampsia | Budd-Chiari Syndrome | Zellweger Syndrome | Metatropic Dysplasia | Kindler Syndrome | Perivascular Epithelioid Cell Tumor | Lymphedema | Acromegaly | Guttate Psoriasis | Arteriosclerosis | Congenital Disorders Of Glycosylation | Erythema Nodosum | Desbuquois Syndrome | Inflammatory Bowel Disease | Orotic Aciduria | Walker-Warburg Syndrome | Plasma Cell Dyscrasia | Progressive Familial Intrahepatic Cholestasis Type 1 | Echinococcosis | Jawad Syndrome | Vascular Cognitive Impairment | Dysplastic Nevus | Leishmaniasis, Visceral | HELLP Syndrome | Cholangitis | Japanese Encephalitis | Spinal And Bulbar Muscular Atrophy | Wiedemann-Steiner Syndrome | Stuve-Wiedemann Syndrome | Omenn Syndrome | Jaundice, Obstructive | Intermittent Explosive Disorder | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Osteogenesis Imperfecta Type III | Necrobiosis Lipoidica | Glycogen Storage Disease Type 4 | Herpes Simplex Dermatitis | Mitochondrial Encephalomyopathy | Apert Syndrome | Diamond-Blackfan Anemia | Nicotine Addiction | Renal Failure | Metabolic Diseases | Prurigo Nodularis | Panniculitis | Fraser Syndrome | Bronchiolitis | Bone Marrow Necrosis | Trichomegaly | Spinal Muscular Atrophy Type 2 | Glanzmann Thrombasthenia | Pain | Parapsoriasis | Pelvic Inflammatory Disease | Pigment Dispersion Syndrome | Asthma | Macrophagic Myofasciitis | Hepatitis, Autoimmune | Anosmia, Congenital | Parkinson's Disease | Esophageal Adenocarcinoma | Nephrotic Syndrome | Heterotaxy | Schizophrenia, Paranoid | Pseudomyxoma Peritonei | Heart Failure | Chondrodysplasia Punctata 1, X-linked Recessive | Keratosis | Gray Platelet Syndrome | Adrenoleukodystrophy, X-linked | Benign Recurrent Intrahepatic Cholestasis 1 | Ovarian Hyperstimulation Syndrome | Ophthalmoplegia | Primary Lateral Sclerosis | Polyarteritis Nodosa | Riboflavin Transporter Deficiency Neuronopathy | Ichthyosis Hystrix, Curth-Macklin Type | Lymphedema-distichiasis Syndrome | Botulism | Extramammary Paget's Disease | Myoclonus | Dystonia Musculorum Deformans | Charcot-Marie-Tooth Disease Type 3 | Congenital Tufting Enteropathy | Wieacker-Wolff Syndrome | Hyperferritinemia-cataract Syndrome | Connective Tissue Disorders | Central Core Disease | Metaphyseal Chondrodysplasia, Schmid Type | Dominant Optic Atrophy | Alpha-thalassemia Myelodysplasia Syndrome | Hypogonadism | X-linked Myotubular Myopathy | Fundus Albipunctatus | Schnitzler Syndrome | Spinocerebellar Ataxia Type 15 | Brooke-Spiegler Syndrome | Anorectal Fistula | Diabetes Insipidus | Restless Legs Syndrome | Micro Syndrome | Spondylosis | Cholecystitis | Eosinophilic Asthma | Dupuytren Disease | Basal Ganglia Disease, Biotin-responsive | Glycogen Storage Disease Type 0 | Bruck Syndrome | Corneal Neovascularization | Osteosclerosis | Infectious Diarrhea | Cystitis, Interstitial | Ichthyosis | Cryptococcal Meningitis | Macular Degeneration | Wolfram Syndrome | Ependymoma | Pyruvate Kinase Deficiency | Iron Overload | Chromosome 5q Deletion Syndrome | Muscle Wasting | Tardive Dyskinesia | Babesiosis | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Nanophthalmos | Histiocytosis | Usher Syndrome Type II | Hypotension, Orthostatic | Eczema | Neuroma | Borjeson-Forssman-Lehmann Syndrome | Anorectal Malformations | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Osteomyelitis | Astigmatism | Meckel-Gruber Syndrome | Pyruvate Carboxylase Deficiency Disease | Choroideremia | Necrotizing Autoimmune Myopathy | Tyrosinemia | Neurocutaneous Melanocytosis | Congenital Hemolytic Anemia | Desmosterolosis | Nasodigitoacoustic Syndrome | Acute Coronary Syndrome | Distal Myopathy 2 | Gilbert Syndrome | Cardiomyopathy, Dilated, 1L | Beta-Propeller Protein-associated Neurodegeneration | KBG Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Coloboma | Pitt-Hopkins Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Shock, Cardiogenic | Multiple Myeloma | Leri Pleonosteosis | Non-small Cell Lung Cancer | Bronchiectasis | Erectile Dysfunction | Multiple Sclerosis, Relapsing-remitting | Chronic Beryllium Disease | Klinefelter Syndrome | Graves Disease | Lymphoma, AIDS-related | 3-methylglutaconic Aciduria Type IV | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Sialidosis Type I | Neurodermatitis | Leiomyosarcoma | Fuchs Dystrophy | Cancer, Colon | Photosensitivity | Ganglioglioma | Acanthosis Nigricans | Epidermolytic Hyperkeratosis | Dysfibrinogenemia | Colitis, Microscopic | Congenital Dyserythropoietic Anemia | Carney-Stratakis Syndrome | Chronic Granulomatous Disease | Bipolar Disorder | Amyotrophic Lateral Sclerosis, Juvenile | Microvillus Inclusion Disease | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Noonan Syndrome-like Disorder With Loose Anagen Hair | Antisynthetase Syndrome | Optic Neuropathy, Anterior Ischemic | Globozoospermia | Meningococcal Infections | Medulloblastoma | Gestational Trophoblastic Disease | Acromicric Dysplasia | Goiter, Nodular | Multiple Sclerosis, Chronic Progressive | Endophthalmitis | Cellulitis | Triple A Syndrome | Congenital Bile Acid Synthesis Defect | Angioedema, Acquired | Liebenberg Syndrome | 5-oxoprolinase Deficiency | Atrial Septal Defect | Syncope | Lewy Body Dementia | IgA Deficiency | Neuromyelitis Optica | Rickets | Esotropia | Chronic Granulomatous Disease, X-linked | Fontaine Progeroid Syndrome | Nephrotic Syndrome Type 1 | Peeling Skin Syndrome Type B | Saul-Wilson Syndrome | Palmoplantar Keratoderma | Infertility | Schistosomiasis Mansoni | Osteomalacia | Non-bullous Congenital Ichthyosiform Erythroderma | Spondylolisthesis | Cavitary Optic Disc Anomalies | Menetrier Disease | Adrenal Insufficiency | Sarcoma, Alveolar Soft Part | Combined Malonic And Methylmalonic Acidemia | Papilloma | Precocious Puberty | Primary Aldosteronism | Aplastic Anemia | Protein C Deficiency | Phenylketonuria II | Focal Facial Dermal Dysplasia | Agranulocytosis | Angioedema, Hereditary | Juvenile Myoclonic Epilepsy | Subacute Sclerosing Panencephalitis | Pycnodysostosis | Poikiloderma With Neutropenia | Generalized Epilepsy And Paroxysmal Dyskinesia | Craniometaphyseal Dysplasia | Carcinoma, Squamous Cell | Restrictive Dermopathy | Carcinoma, Signet Ring Cell | Lassa Fever | Large Granular Lymphocytic Leukemia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Chronic Lymphocytic Leukemia | Glaucomatocyclitic Crisis | Myocardial Infarction | Hyperekplexia | Bursitis | Hyperinsulinemic Hypoglycemia | Nemaline Myopathy 8 | Acrodermatitis Enteropathica | Congenital Ichthyosiform Erythroderma | Optic Neuropathy | Familial Retinal Arterial Macroaneurysm | Atopic Dermatitis | Enterocolitis, Necrotizing | Wolman Disease | Androgenic Alopecia | Niemann-Pick Disease, Type C | Tetraplegia | Seminoma | Varices | Leber Hereditary Optic Neuropathy | Mucolipidosis Type III | Pure Autonomic Failure | Autosomal Recessive Spastic Paraplegia Type 75 | HANAC Syndrome | Glycogen Storage Disease Type 6 | Kleine-Levin Syndrome | Keratitis-ichthyosis-deafness Syndrome | Hereditary Coproporphyria | Histoplasmosis | Lysosomal Acid Lipase Deficiency | Giant Cell Arteritis | Hemorrhagic Disorders | Addison Disease | Localized Scleroderma | Porphyria, Acute Intermittent | Anti-NMDA Receptor Encephalitis | Wiskott-Aldrich Syndrome | Amelanotic Melanoma | Spondyloperipheral Dysplasia | Hypertelorism | L-2-Hydroxyglutaric Aciduria | Seborrheic Dermatitis | Pseudoexfoliation Syndrome | Hemorrhage | Sclerosteosis | AIDS Dementia Complex | Pancytopenia | Fabry's Disease | Epilepsy | 3-methylglutaconic Aciduria Type I | Intermittent Claudication | Brugada Syndrome 1 | Hernia, Inguinal | Cranioectodermal Dysplasia | Diabetes Gestational | Peripheral Neuropathy | Headache | Chondrodysplasia Punctata | Glaucoma, Congenital | Angioimmunoblastic T-cell Lymphoma | Panuveitis | Amblyopia | Diarrhea | Greenberg Dysplasia | Vertebrobasilar Insufficiency | DOCK8 Immunodeficiency Syndrome | NGLY1 Deficiency | Relapsing Polychondritis | Pneumoconiosis | Congenital Hereditary Endothelial Dystrophy Type II | Schwartz-Jampel-Aberfeld Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Inflammatory Myopathy | Progressive Familial Intrahepatic Cholestasis | Meconium Ileus | Duodenal Atresia | Cranial Nerve Disease | Orthostatic Intolerance | Opisthorchiasis | Van Der Knaap Disease | Antisocial Personality Disorder | Pernicious Anemia | Episodic Ataxia | Exfoliative Dermatitis | Congenital Heart Block | Alpha-1 Antitrypsin Deficiency | Vitamin A Deficiency | Spina Bifida | Klippel-Feil Syndrome | Brenner Tumor | Donnai-Barrow Syndrome | Rotor Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Congenital Nystagmus | Stargardt Disease | Melanoma, Uveal | Charcot-Marie-Tooth Disease Type 4 | Corneal Edema | Polycystic Ovary Syndrome | Leukoplakia, Oral | Creatine Deficiency Syndrome Due To AGAT Deficiency | Sclerosing Cholangitis | Chronic Myelomonocytic Leukemia | Patent Foramen Ovale | Tay-Sachs Disease | Hemangioma | Fanconi Anemia | Dysmorphophobia | Glaucoma | Hyperparathyroidism-jaw Tumor Syndrome | Palsy, Cerebral | Waardenburg Syndrome Type 2A | Anemia | Cold Agglutinin Disease | Sleep Apnea | Congenital Fiber-type Disproportion Myopathy | Gerodermia Osteodysplastica | Facioscapulohumeral Muscular Dystrophy | Melanoma, Malignant | Chronic Periodontitis | Pyruvate Dehydrogenase Deficiency | Episodic Ataxia Type 2 | Keratosis, Actinic