Mucolipidosis Type III

About the Disease
Mucolipidosis Iii Gamma, also known as mucolipidosis type iii gamma, is related to mucolipidoses and mucolipidosis, and has symptoms including stiff shoulders, thick skin and arthralgia. An important gene associated with Mucolipidosis Iii Gamma is GNPTG (N-Acetylglucosamine-1-Phosphate Transferase Subunit Gamma). The drug polysaccharide-K has been mentioned in the context of this disorder. Affiliated tissues include bone, heart and eye, and related phenotypes are craniofacial hyperostosis and hypoplastic inferior ilia

Common Targets
GNPTAB | GNPTG | IDUA

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

Other Diseases

Stromal Corneal Dystrophy | Sickle Cell Disease | Rothmund-Thomson Syndrome | SAPHO Syndrome | Bulimia Nervosa | Light Chain Amyloidosis | Familial Hyperaldosteronism | Echinococcosis | Photosensitivity | Alopecia | Syncope | Gerstmann-Straussler-Scheinker Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Delayed Sleep Phase Syndrome | Liebenberg Syndrome | Menetrier Disease | Adenosine Deaminase Deficiency | Epidermolysis Bullosa Simplex, Localized | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Arthritis, Gouty | Spondylosis | Fascioliasis | Urofacial Syndrome | Congenital Hypofibrinogenemia | Thromboembolism | Traboulsi Syndrome | Vascular Calcification | Protein S Deficiency | Epiphyseal Chondrodysplasia, Miura Type | Osteogenesis Imperfecta Type V | Waardenburg Syndrome Type 1 | Kallmann Syndrome | Smith-Kingsmore Syndrome | Maternally Inherited Diabetes And Deafness | Von Willebrand Disease | Aneurysm, Abdominal Aortic | Liver Failure, Acute Infantile | Coffin-Lowry Syndrome | Congenital Torticollis | Glycogen Storage Disease Type 3 | Angioedema, Acquired | Membranous Nephropathy | KBG Syndrome | Fontaine Progeroid Syndrome | Sporadic Inclusion Body Myositis | Johanson-Blizzard Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Phenylketonuria II | Acute Lymphocytic Leukemia | Williams Syndrome | Jalili Syndrome | Focal Cortical Dysplasia Type 2 | C3 Glomerulonephritis | Impulse Control Disorder | Esthesioneuroblastoma | Kernicterus | Acromesomelic Dysplasia | Bipolar Disorder | Diabetic Neuropathy | Hepatorenal Syndrome | Diverticulitis | Disseminated Superficial Actinic Porokeratosis | Carney-Stratakis Syndrome | Vitamin A Deficiency | Craniofacial Dysostosis | Lentigo | AIDS | Hyperlipidemia, Familial Combined | Myhre Syndrome | Waardenburg Syndrome Type 4A | Leishmaniasis, Visceral | Pure Red Cell Aplasia | Vasculitis | Multiple Sclerosis, Relapsing-remitting | Keratopathy | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Autonomic Nervous System Disorders | Fraser Syndrome | Alzheimer Disease, Late Onset | Trichothiodystrophy | Azoospermia | Neuroectodermal Tumors, Primitive | Toxoplasmosis | Aplastic Anemia | Stickler Syndrome | Thyroid Dyshormonogenesis | Dowling-Degos Disease | Diabetic Encephalopathy | Bietti Crystalline Dystrophy | Cystitis | Synovitis | Ocular Hypertension | Stroke | VACTERL/VATER Association | Persistent Mullerian Duct Syndrome | Nemaline Myopathy | Hypohidrotic Ectodermal Dysplasia, X-linked | Oculodentodigital Dysplasia | Neurocysticercosis | Hemochromatosis | Insulinoma | Fucosidosis | Chondrodysplasia Punctata 2, X-linked Dominant | Gliosarcoma | Familial Advanced Sleep Phase Syndrome | Withdrawal Syndrome | Diabetes Mellitus, Transient Neonatal | Multiple Hamartoma Syndrome | Adams-Oliver Syndrome | Periventricular Leukomalacia | Diabetes Gestational | Familial Hypertrophic Cardiomyopathy | Beta-Propeller Protein-associated Neurodegeneration | Omenn Syndrome | Meesmann Corneal Dystrophy | Klinefelter Syndrome | Partington Syndrome | Lung Diseases | Dysfibrinogenemia | Vitamin K Deficiency | Nemaline Myopathy 10 | Osmotic Demyelination Syndrome | Glycogen Storage Disease Type 0, Muscle | Fatty Aldehyde Dehydrogenase Deficiency | Empyema | Craniosynostosis | Haim-Munk Syndrome | Varices | 3-M Syndrome | Subacute Sclerosing Panencephalitis | Alexander Disease | Salla Disease | Urolithiasis | Bone Giant Cell Tumor | Arthritis, Reactive | Creutzfeldt-Jakob Disease | Fowler's Syndrome | Thyroid Hormone Resistance | Glaucomatocyclitic Crisis | Lyme Disease | Ileitis | Agranulocytosis | Guttate Psoriasis | Oligoastrocytoma | Cerebrotendinous Xanthomatosis | Sengers Syndrome | Stiff-man Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Gallstones | Hyper IgE Syndrome | Corneal Neovascularization | Polycythemia | Long QT Syndrome Type 3 | X-linked Acrogigantism | Autoimmune Hemolytic Anemia | Allan-Herndon-Dudley Syndrome | Lewy Body Dementia | Erythromelalgia | Pseudohermaphroditism | Blood Protein Disorders | Intermittent Claudication | Carcinoid Tumor | Niemann-Pick Disease, Type B | Prune Belly Syndrome | Hyperhomocysteinemia | Choroiditis | Intestinal Tuberculosis | Greenberg Dysplasia | Charcot-Marie-Tooth Disease Type 2D | Blepharitis | Common Cold | Smoldering Myeloma | Viral Meningitis | Glutaric Aciduria Type 1 | Polyneuropathy | Sleep Apnea, Obstructive | Fibrodysplasia Ossificans Progressiva | Focal Dermal Hypoplasia | Seasonal Mood Disorder | Spinocerebellar Ataxia Type 16 | Renal Tubular Dysgenesis | Usher Syndrome Type I | Carcinoma, Squamous Cell | Raine Syndrome | Argininosuccinic Aciduria | Carney Triad | Pernicious Anemia | Hepatitis D | Purpura | Congenital Stromal Corneal Dystrophy | Acrodermatitis Enteropathica | Potocki-Shaffer Syndrome | IMAGe Syndrome | Language Disorders | Acute Leukemia | Herpes Genitalis | Sick Sinus Syndrome 1 | DICER1 Syndrome | Tremor | Noonan Syndrome | Pemphigus Vulgaris | Hemangioblastoma | Brachial Plexus Neuropathy | Hemolytic Anemia | Neuromuscular Disorders | Borderline Personality Disorder | Angiosarcoma | Hepatic Adenomatosis | Optic Nerve Diseases | Myelomeningocele | Spondyloarthritis | Van Der Knaap Disease | Splenomegaly | Schizotypal Personality Disorder | Hypertriglyceridemia | Recurrent Respiratory Papillomatosis | Superficial Spreading Melanoma | Anterior Segment Dysgenesis | Combined Malonic And Methylmalonic Acidemia | Asthma, Exercise-induced | Lamellar Ichthyosis | Chronic Periodontitis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Ebstein Anomaly | Osteomalacia | Renal Medullary Carcinoma | PHARC Syndrome | Brooke-Spiegler Syndrome | Arthrogryposis | Lennox-Gastaut Syndrome | Gastroschisis | Cataplexy | Pseudoachondroplasia | Rickets | McLeod Syndrome | Gray Platelet Syndrome | Hypertelorism | Hyperuricemia | Norrie Disease | Gilbert Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Acute Tubular Necrosis | Anal Fissure | Intestinal Hypomagnesemia 1 | Antley-Bixler Syndrome | Hydrops Fetalis | Polycystic Kidney, Autosomal Recessive | Dyskeratosis Congenita | Peripheral T-cell Lymphoma | Aceruloplasminemia | Neurofibromatosis Type 2 | Binge Eating Disorder | Fahr Disease | Heterotaxy | Erythema Nodosum | Schnyder Crystalline Corneal Dystrophy | Lipid Storage Myopathy | Transthyretin-related Amyloidosis | Deafness, Dystonia, And Cerebral Hypomyelination | Hereditary Hemorrhagic Telangiectasia | Herpes Simplex Dermatitis | Duodenal Atresia | CREST Syndrome | Congenital Mirror Movements | Ulcerative Colitis | Congestive Heart Failure | Mitochondrial DNA Depletion Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Parkinson Disease 6, Autosomal Recessive Early-onset | Diabetes | Pericarditis | Gangliosidosis, GM1 | Precocious Puberty | Episodic Ataxia Type 2 | Multiple Myeloma | Hypolipoproteinemia | Keratocystic Odontogenic Tumor | Temporal Lobe Epilepsy | Apraxia | Ehlers-Danlos Syndrome | T-cell Chronic Lymphocytic Leukemia | Keloid | Bainbridge-Ropers Syndrome | Hypertension, Portal | Dementia | Parkinson's Disease | Angiosarcoma Of The Breast | Diffuse Mesangial Sclerosis | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Cirrhosis | Epilepsy Of Infancy With Migrating Focal Seizures | Hepatitis, Autoimmune | Carcinoma, Transitional Cell | Neuroma | Sleep Apnea, Central | Fibromuscular Dysplasia | 3-hydroxy-3-methylglutaric Aciduria | Behavioral Variant Of Frontotemporal Dementia | Clouston Hidrotic Ectodermal Dysplasia | Localized Scleroderma | Blepharo-cheilo-odontic Syndrome | Growth Hormone Excess | Coma | Li-Fraumeni Syndrome | Pyruvate Decarboxylase Deficiency | Myofibrillar Myopathy | Schwannomatosis | Fibronectin Glomerulopathy | Hereditary Xerocytosis | Vitamin B12 Deficiency | Nemaline Myopathy 8 | Sclerosteosis 2 | Crisponi Syndrome | Varicocele | Usher Syndrome Type IIC | Atopic Dermatitis | Oral Lichen Planus | Hemolytic Uremic Syndrome, Atypical | Smith-Magenis Syndrome | Ovarian Sex Cord-stromal Tumor | Keratosis, Actinic | Vici Syndrome | Spinocerebellar Ataxia Type 3 | Osteitis | Hepatic Steatosis | Agnathia-Otocephaly Complex | Macrophagic Myofasciitis | Tetraplegia | CEDNIK Syndrome | Pachyonychia Congenita | Proximal Symphalangism | Ollier Disease | Conjunctivitis, Allergic | Amyotrophic Lateral Sclerosis, Juvenile | Microcephalic Primordial Dwarfism | Nicotine Dependence | Retinal Detachment | Nephrosclerosis | Malnutrition | Constipation | Persistent Truncus Arteriosus | X-linked Sideroblastic Anemia | Hyperinsulinism-hyperammonemia Syndrome | Amenorrhea | Heimler Syndrome | Fabry's Disease | Still Disease | Duchenne Muscular Dystrophy | Platelet Disorders | Progressive Familial Intrahepatic Cholestasis Type 3 | Hydrocephalus, Normal Pressure | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Pouchitis | Short-chain Acyl-CoA Dehydrogenase Deficiency | Intracranial Hypertension | Mucolipidosis | Exostoses | Peripheral Neuropathy | Malaria | GATA2 Deficiency | Scapuloperoneal Spinal Muscular Atrophy | Multisystemic Smooth Muscle Dysfunction Syndrome | Fukuyama Congenital Muscular Dystrophy | Lymphomatoid Granulomatosis | Retinal Degeneration | Congenital Primary Aphakia | Dubin-Johnson Syndrome | Hepatitis, Alcoholic | Spinocerebellar Ataxia Type 31 | Proctitis | Polyradiculopathy | Phosphoglycerate Dehydrogenase Deficiency | Blue Rubber Bleb Nevus Syndrome | Macular Corneal Dystrophy | Charcot-Marie-Tooth Disease, Type 2C | Marinesco-Sjogren Syndrome | Adenomatoid Tumor | Dermatofibrosarcoma | Ghosal Syndrome | Oculopharyngeal Muscular Dystrophy | Heavy Chain Disease | Speech Disorders | Otitis Externa | Waardenburg Syndrome Type 2E | Achondrogenesis | Infantile Liver Failure Syndrome 1 | Sick Sinus Syndrome | Rash | Eiken Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Multiple Sclerosis, Chronic Progressive | Pontocerebellar Hypoplasia Type 2 | Multicystic Renal Dysplasia | Paraplegia | Primary Biliary Cholangitis | Hypertrophy | Mandibuloacral Dysplasia With Type A Lipodystrophy | Neurocutaneous Syndromes | Torticollis | Non-proliferative Diabetic Retinopathy