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.tech.

Other Diseases

Acute Coronary Syndrome | Reticular Dysgenesis | Melanoma, Uveal | Pseudo-pseudohypoparathyroidism | Urticaria | Mucolipidosis Type II | Follicular Dendritic Cell Sarcoma | Chorioretinitis | Familial Pheochromocytoma-paraganglioma | Clouston Hidrotic Ectodermal Dysplasia | Tardive Dyskinesia | Hypobetalipoproteinemias | AIDS | Ureteropelvic Junction Obstruction | Supravalvular Aortic Stenosis | Colorectal Adenoma | Coma | Adrenoleukodystrophy, X-linked | Rotor Syndrome | Pulmonary Sclerosing Hemangioma | Cardiomyopathy, Restrictive | Tetraplegia | Barakat Syndrome | Ebstein Anomaly | Enlarged Vestibular Aqueduct | Hypodontia | Asthma, Nocturnal | Mosaic Variegated Aneuploidy Syndrome 2 | Leri-Weill Dyschondrosteosis | Intracerebral Hemorrhage | Epiphyseal Chondrodysplasia, Miura Type | Vitiligo | Immunoproliferative Disorders | Pre-eclampsia | Metatropic Dysplasia | Acrodermatitis Enteropathica | Familial Exudative Vitreoretinopathy | Mucolipidosis | Inflammatory Joint Disease | Multiple Sclerosis, Relapsing-remitting | Acute Chest Syndrome | Hypohidrotic Ectodermal Dysplasia, X-linked | Cholelithiasis | Hyperbilirubinemia, Neonatal | Glycogen Storage Disease Type 1a | Pyruvate Dehydrogenase Deficiency | Familial Hypertrophic Cardiomyopathy | Phosphoglycerate Dehydrogenase Deficiency | Lipodystrophy | Ichthyosis Hystrix, Curth-Macklin Type | Conduct Disorder | Alcoholism | Nephropathy | Systemic Lupus Erythematosus | Fanconi Anemia | Hyperlipidemia Type V | Hashimoto Thyroiditis | Ectrodactyly | Hypohidrotic Ectodermal Dysplasia | Gangliosidosis | Thrombotic Microangiopathy | Erythema Nodosum | Primary Hyperoxaluria | Takayasu's Arteritis | Poretti-Boltshauser Syndrome | Ulcerative Colitis | Hypereosinophilic Syndrome | Paroxysmal Kinesigenic Dyskinesia | Pleural Tuberculosis | Porphyria, Acute Intermittent | Malignant Peripheral Nerve Sheath Tumor | Congenital Myasthenic Syndrome | Retinal Degeneration | Anxiety Disorders | Tumoral Calcinosis | Cholecystitis | Teratozoospermia | Erectile Dysfunction | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Lateral Meningocele Syndrome | Antisocial Personality Disorder | Anovulation | Melanoma | Osteogenesis Imperfecta Type VI | Li-Fraumeni Syndrome | Carcinoma, Squamous Cell | Primary Sclerosing Cholangitis | Polyomavirus Nephropathy | Basal Cell Nevus Syndrome | Persistent Mullerian Duct Syndrome | Compartment Syndrome | Measles | Facioscapulohumeral Muscular Dystrophy Type 1 | Angiosarcoma Of The Breast | Raynaud Phenomenon | Oculocutaneous Albinism Type 2 | Spondylometaphyseal Dysplasia | Scleroderma | Blomstrand Osteochondrodysplasia | Chronic Lymphocytic Leukemia | Ependymoma | HIBCH Deficiency | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Craniolenticulosutural Dysplasia | Vascular Cognitive Impairment | Primary Torsion Dystonia | X-linked Acrogigantism | Goiter | Adenomatoid Tumor | Trichomegaly | Charcot-Marie-Tooth Disease | Protein C Deficiency | AIDS Dementia Complex | Long QT Syndrome Type 3 | Crimean-Congo Hemorrhagic Fever | Pterygium | Cervical Dystonia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Dysferlinopathy | Tremor | Limb Girdle Muscular Dystrophy | Trichorhinophalangeal Syndrome | Amish Infantile Epilepsy Syndrome | Asphyxia Neonatorum | Leukoencephalopathy, Progressive Multifocal | Bronchiolitis | Angiodysplasia | Hypertension, Essential | C3 Glomerulonephritis | Greenberg Dysplasia | Inflammatory Linear Verrucous Epidermal Nevus | Congenital Bile Acid Synthesis Defect | Pyruvate Decarboxylase Deficiency | Cockayne Syndrome | Cutaneous Angiosarcoma | Amenorrhea | Joubert Syndrome | Osteonecrosis Of The Jaw | Reye Syndrome | Methylmalonic Acidemia | Acne Vulgaris | Duane Retraction Syndrome | Peutz-Jeghers Syndrome | Tyrosinemia Type 1 | Hypothyroidism | Erythrokeratodermia Variabilis | Kleine-Levin Syndrome | Rift Valley Fever | Pneumothorax | Cutis Laxa | Hemophilia | Usher Syndrome | LMNA-related Congenital Muscular Dystrophy | Trichothiodystrophy | Neuroectodermal Tumors, Primitive | Hyperinsulinism-hyperammonemia Syndrome | Osteochondrosis | Dysequilibrium Syndrome | Glanzmann Thrombasthenia | Keratosis, Actinic | Infertility | Hepatic Veno-occlusive Disease | Retinopathy Of Prematurity | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Acrodermatitis | Hyperinsulinemia | Glaucomatocyclitic Crisis | Congenital Stationary Night Blindness | Angiosarcoma | Hyperkeratosis | Eating Disorder | Sarcosinemia | Isobutyryl-CoA Dehydrogenase Deficiency | Congenital Afibrinogenemia | Cerebellofaciodental Syndrome | Tyrosinemia | Corneal Dystrophy | Basal Ganglia Disease | Epidermolytic Hyperkeratosis | Cardiomyopathy, Hypertrophic | Focal Facial Dermal Dysplasia | Encephalocele | Cone Dystrophy | Spondylolisthesis | Nestor-Guillermo Progeria Syndrome | Gastroenteritis | Usher Syndrome Type III | Ectodermal Dysplasia | Acral Lentiginous Melanoma | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Liver Failure, Acute Infantile | Glutathione Synthetase Deficiency | 3-methylcrotonyl-CoA Carboxylase Deficiency | Spinocerebellar Ataxia Type 27 | Charcot-Marie-Tooth Disease Type 4 | Frontotemporal Dementia | Amyloidosis | Raine Syndrome | Christianson Syndrome | Cyst | Arthritis, Gouty | Adult Polyglucosan Body Disease | Cyclic Vomiting Syndrome | Dent Disease | Glomerulonephritis, Membranous | Abetalipoproteinemia | Pemphigus Foliaceus | Liebenberg Syndrome | Brenner Tumor | Empyema | Jalili Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Sleep Apnea | Schizophrenia | Heart Septal Defects | Irritable Bowel Syndrome | Myoclonus-dystonia Syndrome | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Chromosome 5q Deletion Syndrome | Hypercalcemia | Ovarian Sex Cord-stromal Tumor | Hereditary Coproporphyria | Granular Corneal Dystrophy Type 1 | Hereditary Pyropoikilocytosis | Miyoshi Myopathy | Carcinoid Syndrome | Lymphangiomatosis | Kallmann Syndrome | Absence Epilepsy | Hepatitis | Spinal Muscular Atrophy | Multiple Myeloma | X-linked Sideroblastic Anemia | Renal Tubular Acidosis | Infantile Nephropathic Cystinosis | Polycystic Kidney, Autosomal Recessive | Enhanced S-cone Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Chromosome 16p11.2 Deletion Syndrome | Hemoglobinopathies | Nance-Horan Syndrome | Ganglioneuroma | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Blue Rubber Bleb Nevus Syndrome | Cat Eye Syndrome | Bulimia Nervosa | Hyperlipidemia | Charcot-Marie-Tooth Disease Type 2E | Renal Hypouricemia | Optic Nerve Diseases | Scapuloperoneal Myopathy, X-linked Dominant | Cancer, Bladder | Early Infantile Epileptic Encephalopathy | Obesity, Morbid | Bullous Pemphigoid | Episodic Ataxia Type 1 | Schaaf-Yang Syndrome | Axenfeld-Rieger Syndrome | Epidermolysis Bullosa | Diabetes Gestational | Epilepsy | Osteoporosis-pseudoglioma Syndrome | Genee-Wiedemann Syndrome | Cholera | Melanocytic Nevus | Vaginitis | Renal Failure | Metachromatic Leukodystrophy | Pulmonary Vein Stenosis | Portal Vein Thrombosis | Intracranial Hypertension | Myasthenia | Anorectal Malformations | Chloridorrhea, Congenital | Optic Atrophy 2 | Congenital Fiber-type Disproportion Myopathy | Papillorenal Syndrome | Arthrogryposis | Antenatal Bartter Syndrome Type 1 | Erythromelalgia | Major Depression | Myotonic Disorders | Aarskog-Scott Syndrome | Vasculitis | DEND Syndrome | Polycythemia Vera | Spinocerebellar Ataxia Type 13 | Multiple Hamartoma Syndrome | Congenital Nephrotic Syndrome | McLeod Syndrome | Synovitis | Hereditary Folate Malabsorption | Nemaline Myopathy 10 | Hypervalinemia | Krabbe Disease | Lymphedema | Stromal Corneal Dystrophy | Oculocutaneous Albinism | Encephalopathy, Glycine | Congenital Sodium Diarrhea | Chondrodysplasia Punctata | Diamond-Blackfan Anemia | Iron Deficiency Anemia | Mast Cell Leukemia | Pernicious Anemia | Polycystic Liver | Gastrointestinal Disorders | POEMS Syndrome | Alpha-mannosidosis | Colitis, Lymphocytic | Chiari Malformation Type I | Adenoma, Pleomorphic | Cardiac Sarcoidosis | Plasma Cell Leukemia | Kidney Stones | Adenoid Cystic Carcinoma | Campomelic Dysplasia | Carcinoma, Small Cell | Alpha-1 Antitrypsin Deficiency | Marinesco-Sjogren Syndrome | Methemoglobinemia | Spermatocele | Phenylketonuria II | Retinoschisis | Dyslipidemia | Hartnup Disease | Corticobasal Syndrome | Ichthyosis, X-linked | Retinal Dystrophy, Early-onset Severe | Brachydactyly | Otopalatodigital Syndrome Type 2 | Hereditary Neuropathy With Liability To Pressure Palsies | Hereditary Spastic Paraplegia | Cole-Carpenter Syndrome | Endocarditis | Oguchi Disease-2 | Familial Male-limited Precocious Puberty | Alpers Syndrome | Leukoplakia | Progressive Osseous Heteroplasia | Charcot-Marie-Tooth Disease Type 4B1 | Stuttering | Dementia | Mitochondrial Disease | Congenital Central Hypoventilation Syndrome | Familial Hemiplegic Migraine | Iron Metabolism Disorders | Autonomic Neuropathy | Congenital Disorders Of Glycosylation | Aldosteronism | HELLP Syndrome | Osteogenesis Imperfecta Type II | Mood Disorder | Arteriovenous Malformations | Mesothelioma, Malignant | Hyperhomocysteinemia | Leishmaniasis, Visceral | Temtamy Preaxial Brachydactyly Syndrome | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Lassa Fever | Mitochondrial DNA Depletion Syndrome 13 | Camurati-Engelmann Disease | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Premature Ejaculation | Dubin-Johnson Syndrome | Common Cold | Motor Neuron Diseases | Fetal And Neonatal Alloimmune Thrombocytopenia | Pontocerebellar Hypoplasia Type 2 | Pulmonary Alveolar Proteinosis | Thyrotoxic Periodic Paralysis | Chanarin-Dorfman Syndrome | Nephrocalcinosis | Joubert Syndrome 2 | Epidermolysis Bullosa Simplex, Generalized | Microphthalmia | Congenital Aniridia | Twin-to-twin Transfusion Syndrome | Farber Disease | Lafora Disease | Osteochondroma | Incontinentia Pigmenti | Primary Familial Brain Calcification | Jawad Syndrome | Schnitzler Syndrome | Cryptococcal Meningitis | Amyotrophic Lateral Sclerosis | Myotonia | Hyperuricemic Nephropathy, Familial Juvenile | Myocarditis | Myasthenia Gravis | Pseudoexfoliation Syndrome | Greig Cephalopolysyndactyly Syndrome | Congenital Torticollis | Neurofibrosarcoma | Hydrops Fetalis | Glycogen Storage Disease Type 3 | Spinal Cord Diseases | Aldosterone Deficiency | Nevus