Mucolipidosis

About the Disease
Mucolipidosis is related to mucolipidosis iii gamma and mucolipidosis iii alpha/beta. An important gene associated with Mucolipidosis is GNPTAB (N-Acetylglucosamine-1-Phosphate Transferase Subunits Alpha And Beta), and among its related pathways/superpathways are Transport to the Golgi and subsequent modification and Ion channel transport. The drugs Prednisolone phosphate and Prednisolone acetate have been mentioned in the context of this disorder. Affiliated tissues include skin, bone and bone marrow, and related phenotypes are no effect and no effect

Common Targets
MCOLN1 | GNPTAB | GNPTG

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

Other Diseases

Opisthorchiasis | Low Tension Glaucoma | Irritable Bowel Syndrome | Benign Familial Neonatal Convulsions | Bronchiectasis | Uremia | Takenouchi-Kosaki Syndrome | Antenatal Bartter Syndrome Type 1 | Cellulitis | Osteochondroma | Auriculocondylar Syndrome | Cystitis | Acral Lentiginous Melanoma | Adrenal Insufficiency | Platelet Disorders | Niemann-Pick Disease, Type A | Vitamin K Deficiency | Huntington's Disease | Giant Axonal Neuropathy | Raine Syndrome | Learning Disability | Best Macular Dystrophy | Perry Syndrome | Triple A Syndrome | Cataplexy | Basan Syndrome | Graft-versus-host Disease | Polyneuropathy | Glutaric Aciduria Type 2 | Blomstrand Osteochondrodysplasia | Spinal Muscular Atrophy Type 2 | Hermansky-Pudlak Syndrome | Hypercholesterolemia, Familial | Anterior Segment Dysgenesis | Coenzyme Q10 Deficiency | Esophageal Carcinoma | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hepatitis, Alcoholic | Feingold Syndrome | Papilledema | Calcium Pyrophosphate Deposition Disease | Schizotypal Personality Disorder | Meier-Gorlin Syndrome | Pityriasis Rubra Pilaris | Thyrotoxic Periodic Paralysis | Pontocerebellar Hypoplasia Type 7 | Thanatophoric Dysplasia | PASLI Disease | Porokeratosis | Leri Pleonosteosis | Craniopharyngioma | Hernia, Inguinal | Gastritis, Atrophic | Dysmorphophobia | Polycystic Kidney, Autosomal Recessive | Progressive Osseous Heteroplasia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Cabezas Syndrome | Pseudohypoparathyroidism Type 1C | Chanarin-Dorfman Syndrome | Celiac Disease | Tracheal Disorders | Chitayat Syndrome | Charcot-Marie-Tooth Disease, Type 2 | Panuveitis | Exostoses | Tyrosinemia Type 2 | Cyclic Vomiting Syndrome | Tardive Dyskinesia | Shwachman-Bodian-Diamond Syndrome | Pierre Robin Syndrome | Palmoplantar Keratoderma | ADNP Syndrome | Retinal Degeneration | Hyperthyroidism | Congestive Heart Failure | Primary Progressive Nonfluent Aphasia | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Lymphomatoid Granulomatosis | Primary Progressive Aphasia | Methemoglobinemia | Neurocysticercosis | Vitamin D Deficiency | Chronic Periodontitis | Lentigo | Rift Valley Fever | Creutzfeldt-Jakob Disease | Wolman Disease | Hepatitis C, Chronic | Bronchiolitis | Non-proliferative Diabetic Retinopathy | Wolff-Parkinson-White Syndrome | Sleep Disorder | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Joubert Syndrome 2 | Encephalopathy, Ethylmalonic | Giant Cell Arteritis | Spermatocele | Blepharoconjunctivitis | Coffin-Siris Syndrome | Hydrops Fetalis | Myelitis | Spinocerebellar Ataxia Type 5 | Premenstrual Syndrome | Primary Pigmented Nodular Adrenocortical Disease | Esthesioneuroblastoma | Chromosome 8q21.11 Deletion Syndrome | Open-angle Glaucoma | Neurofibromatosis | Myeloid Leukemia | Epidermodysplasia Verruciformis | Spina Bifida | Mevalonate Kinase Deficiency | Pemphigus Vulgaris | Chronic Idiopathic Myelofibrosis | Familial Hypertrophic Cardiomyopathy | Neurodegeneration With Brain Iron Accumulation | Trigonocephaly | Progressive External Ophthalmoplegia | Trichomegaly | Oculocutaneous Albinism Type 1 | Diamond-Blackfan Anemia | Microcephaly | Long QT Syndrome Type 2 | Primary Aldosteronism | Short-chain Acyl-CoA Dehydrogenase Deficiency | Exfoliative Dermatitis | Liver Diseases | Poretti-Boltshauser Syndrome | Vaginitis | Spondyloperipheral Dysplasia | Sclerocornea | Androgenic Alopecia | Focal Dermal Hypoplasia | Peeling Skin Syndrome Type B | Currarino Syndrome | Paraganglioma | Amblyopia | Chronic Granulomatous Disease | Neurofibroma, Plexiform | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Peripheral Neuropathy | HELLP Syndrome | Atherosclerosis | Myasthenia | Hereditary Folate Malabsorption | Congenital Diaphragmatic Hernia | Cysticercosis | Schwannomatosis | Lymphopenia | Nephritis, Interstitial | Retinal Diseases | Goiter | D-2-Hydroxyglutaric Aciduria | Emery-Dreifuss Muscular Dystrophy | Multicentric Carpotarsal Osteolysis Syndrome | Renal Oncocytoma | Intermittent Claudication | Ellis-Van Creveld Syndrome | Spinocerebellar Ataxia Type 3 | Palsy, Cerebral | Hypercalcemia | Bartsocas-Papas Syndrome | Oculodentodigital Dysplasia | Thin Basement Membrane Disease | Cantu Syndrome | Peyronie's Disease | Polymicrogyria | Stomatitis | Glaucoma, Congenital | Ischemia | Meningococcal Meningitis | Hypersomnia | Lipid Storage Myopathy | Encephalitis | Phosphoglycerate Dehydrogenase Deficiency | Renal Hypouricemia | Pseudohypoparathyroidism Type 1A | Carcinoma In Situ | Adenoid Cystic Carcinoma | Bainbridge-Ropers Syndrome | Dental Caries | Kleine-Levin Syndrome | Hemolytic Anemia | Cutis Laxa | Cervical Dystonia | Spondylocostal Dysostosis | Medulloblastoma | Anemia | Keratosis, Seborrheic | Hypopituitarism | Spinocerebellar Ataxia Type 27 | Porphyria | Mucolipidosis Type IV | Fibromyalgia | Arthritis, Psoriatic | Peroxisomal Disorder | Gaucher Disease | Papillorenal Syndrome | Macrophagic Myofasciitis | Portal Vein Thrombosis | Granular Corneal Dystrophy | Gastric Atrophy | Primary Lateral Sclerosis | Colitis, Microscopic | Roberts Syndrome | Hereditary Coproporphyria | Blue Rubber Bleb Nevus Syndrome | Retinopathy Of Prematurity | Premature Ejaculation | Superficial Spreading Melanoma | Neuromyotonia | Lymphoma, AIDS-related | Antley-Bixler Syndrome | Nephrotic Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Systemic Mastocytosis | Niemann-Pick Disease, Type C | Tonsillitis | Empyema | Desbuquois Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Agnathia-Otocephaly Complex | Methylmalonic Acidemia | Gilbert Syndrome | Hyperglycemia | Hairy Cell Leukemia | Epilepsy | Mucolipidosis | Nephropathy | Smith-Magenis Syndrome | Treacher Collins Syndrome | Primary Hyperoxaluria Type 3 | Anovulation | Pernicious Anemia | Chordoid Glioma | Hemorrhage | Periodontitis | Impetigo | Poirier-Bienvenu Neurodevelopmental Syndrome | Orotic Aciduria | T-cell Prolymphocytic Leukemia | FG Syndrome | Spondylo-ocular Syndrome | Acute Tubular Necrosis | Osteoporosis-pseudoglioma Syndrome | Cherubism | Albinism | Sarcoma | Achromatopsia | Carbohydrate Metabolism Disorders | Arthritis, Gouty | Tendinopathy | Central Pain Syndrome | Double Outlet Right Ventricle | Diabetes | Hypermethioninemia | GM2-gangliosidosis AB Variant | Diabetes Type 1 | Cousin Syndrome | Neurodevelopmental Disorders | Pheochromocytoma | Pendred Syndrome | Polycystic Liver | Ebstein Anomaly | Azoospermia | Hereditary Multiple Exostoses | Diastrophic Dysplasia | Pemphigus Foliaceus | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Cone Dystrophy | Proteus Syndrome | Crisponi Syndrome | Intestinal Obstruction | Inflammatory Joint Disease | Glycogen Storage Disease Type 1 | Spondylolisthesis | Molybdenum Cofactor Deficiency | Priapism | Fibrodysplasia Ossificans Progressiva | Pearson Syndrome | Sarcoma, Endometrial Stromal | Kawasaki Disease | Glutaric Aciduria Type 3 | Epilepsy Of Infancy With Migrating Focal Seizures | Carey-Fineman-Ziter Syndrome | Unverricht-Lundborg Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Lymphoma, Follicular | Paget's Disease Of The Breast | Yellow Fever | Uveitis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Chylomicron Retention Disease | Occipital Neuralgia | Amyotrophic Lateral Sclerosis | Chromosome 17q21.31 Deletion Syndrome | Waardenburg Syndrome Type 4A | Blepharospasm | DOCK8 Immunodeficiency Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Stickler Syndrome | Dysequilibrium Syndrome | Hypertriglyceridemia | Kohlschutter-Tonz Syndrome | Eccrine Porocarcinoma | Hypertension, Portal | Jalili Syndrome | Alagille Syndrome | Hepatitis D | Mesothelioma, Malignant | Congenital Hereditary Endothelial Dystrophy Type I | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Hypereosinophilic Syndrome | Congenital Myopathy | Desmosterolosis | Acromicric Dysplasia | Chudley-McCullough Syndrome | Pseudo-pseudohypoparathyroidism | Acute Motor Axonal Neuropathy | Nephroblastoma | Retinal Vasculitis | Hypoglycemia | Tangier Disease | Seborrheic Dermatitis | Meniere's Disease | Carcinoma, Merkel Cell | Chondromyxoid Fibroma | Shock, Cardiogenic | Bronchitis, Chronic | Carcinoma, Squamous Cell | Primary Sclerosing Cholangitis | Endophthalmitis | Choroideremia | Corneal Dystrophies, Hereditary | Spinocerebellar Ataxia Type 42 | Sjogren Syndrome | Mumps | GAPO Syndrome | Precocious Puberty | DRESS Syndrome | Fascioliasis | Iron Metabolism Disorders | C3 Glomerulopathy | Tuberculous Meningitis | Lymphangioleiomyomatosis | Leber Congenital Amaurosis | Mandibuloacral Dysplasia With Type A Lipodystrophy | Spondylometaphyseal Dysplasia | Neurocutaneous Melanocytosis | Avellino Corneal Dystrophy | Autosomal Recessive Bestrophinopathy | Achondrogenesis | Spinal And Bulbar Muscular Atrophy | Synpolydactyly | Acute Kidney Injury | Multiple Epiphyseal Dysplasia | Vasculitis | Fibrosarcoma | Tic Disorder | Micropenis | Hennekam Lymphangiectasia-lymphedema Syndrome | Esophagitis | Myositis | Progressive Familial Intrahepatic Cholestasis Type 1 | Behcet's Disease | Thyroid Hormone Resistance | Arteriovenous Malformations | Borderline Personality Disorder | Atopy | Proopiomelanocortin Deficiency | Rhinitis | Amyloidosis | Oculocutaneous Albinism Type 2 | Mitochondrial Myopathy | Frontotemporal Dementia | Chronic Leukemia | Fatty Aldehyde Dehydrogenase Deficiency | Diabetes Gestational | Fabry's Disease | Ophthalmoplegia | Colorectal Adenoma | Asthma, Nocturnal | Gestational Trophoblastic Disease | Chronic Myeloid Leukemia | Cerebrovascular Disorders | Aplasia Cutis Congenita | Blau Syndrome | Hamartoma | Hyperprolactinemia | Phenylketonuria II | Metachondromatosis | Agoraphobia | Histoplasmosis | Localized Scleroderma | Anorectal Fistula | Keratoacanthoma | Melanoma, Malignant | Osteoglophonic Dysplasia