Disease

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

疾病靶点研报
Mucolipidosis

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

Sarcoma, Ewing | Usher Syndrome Type I | Acute Leukemia | Cutaneous T-cell Lymphoma | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Wiskott-Aldrich Syndrome | Thyrotoxic Periodic Paralysis | Cystitis | Retinitis | Prolidase Deficiency | Postaxial Polydactyly | Oligodendroglioma | Polymyositis | Uveitis | Wolcott-Rallison Syndrome | Hereditary Spherocytosis | Aldosterone Deficiency | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Tuberculous Meningitis | Endocarditis | Polyneuropathy | Lateral Meningocele Syndrome | Specific Granule Deficiency | Posterior Polar Cataract | Nephroblastoma | Myotonic Disorders | Polyomavirus Nephropathy | Syncope | Monilethrix | Corneal Dystrophies, Hereditary | Behavioral Variant Of Frontotemporal Dementia | Stroke, Hemorrhagic | Keratosis, Actinic | 5-oxoprolinase Deficiency | Pemphigoid | Bronchiolitis | HIBCH Deficiency | Diffuse Palmoplantar Keratoderma | Hypereosinophilic Syndrome | Coronary Heart Disease | Facioscapulohumeral Muscular Dystrophy | Hepatitis B, Chronic | Blue Nevus | Fascioliasis | Epidermolysis Bullosa Acquisita | Epidermolysis Bullosa Simplex | Persistent Hyperplastic Primary Vitreous | Pupil Disorders | Axenfeld-Rieger Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Non-Langerhans Cell Histiocytosis | Rolandic Epilepsy | Angioimmunoblastic T-cell Lymphoma | Tricho-hepato-enteric Syndrome | Sarcoma | Greig Cephalopolysyndactyly Syndrome | Endophthalmitis | Absence Epilepsy | IgA Nephropathy | Hyperinsulinemia | Mitochondrial DNA Depletion Syndrome 13 | Birk-Barel Syndrome | Skin Carcinoma | Palsy, Cerebral | Uterine Leiomyoma | Gastroenteritis, Eosinophilic | Spondylosis | Presbyopia | Oculocutaneous Albinism Type 1 | Mucormycosis | Duchenne Muscular Dystrophy | Glycogen Storage Disease Type 1b | Pineoblastoma | Pouchitis | Opisthorchiasis | Dysthymia | Desmosterolosis | Periventricular Nodular Heterotopia | Nephrocalcinosis | Sporadic Hemiplegic Migraine | Optic Neuropathy, Anterior Ischemic | Spondylocarpotarsal Synostosis Syndrome | Maple Syrup Urine Disease | Familial Hypertrophic Cardiomyopathy | Otitis Media | Congenital Tufting Enteropathy | Acromesomelic Dysplasia | Neural Tube Defect | Basan Syndrome | Dubin-Johnson Syndrome | Spinocerebellar Ataxia Type 38 | Melanoma, Malignant | Arts Syndrome | Hypoparathyroidism | Richter's Syndrome | Hypertrophy | Orthostatic Intolerance | Lathosterolosis | Leukoplakia | Strabismus | Meier-Gorlin Syndrome | Autoimmune Polyendocrine Syndrome | Shprintzen-Goldberg Syndrome | Renal Medullary Carcinoma | Yellow Fever | Congenital Muscular Dystrophy | Hypoplastic Left Heart Syndrome | Congenital Diaphragmatic Hernia | Lymphomatoid Granulomatosis | Cancer, Kidney | Carney-Stratakis Syndrome | Recurrent Respiratory Papillomatosis | Multiple Sclerosis, Primary Progressive | Episodic Ataxia | Seizures-scoliosis-macrocephaly Syndrome | Gardner Syndrome | Meningioma | Mohr-Tranebjaerg Syndrome | Congenital Fiber-type Disproportion Myopathy | Fanconi Syndrome | Hemangioblastoma | Moyamoya Disease | Tyrosine Hydroxylase Deficiency | Mitochondrial Cytopathy | Takayasu's Arteritis | Duane Retraction Syndrome | Pityriasis Rubra Pilaris | Progressive Familial Intrahepatic Cholestasis | Eosinophilia | Dental Caries | Takotsubo Cardiomyopathy | Episodic Ataxia Type 2 | Diabetes Insipidus, Neurogenic | Glycogen Storage Disease Type 5 | Chronic Mucocutaneous Candidiasis | Diastrophic Dysplasia | Ameloblastic Carcinoma | Charcot-Marie-Tooth Disease Type 4D | Stroke | Leiomyosarcoma | Marinesco-Sjogren Syndrome | Lamellar Ichthyosis | Anorectal Fistula | Generalized Epilepsy With Febrile Seizures Plus | Dowling-Degos Disease | Infantile Refsum Disease | Vitamin K Deficiency | Pleurisy | Retinoblastoma | Fuchs Dystrophy | Perivascular Epithelioid Cell Tumor | Gastritis, Atrophic | Hemochromatosis Type 1 | Vertigo | Uremic Pruritus | Sleep Apnea | Tylosis With Esophageal Cancer | Short-chain Acyl-CoA Dehydrogenase Deficiency | Osteoporosis-pseudoglioma Syndrome | Fibrosis | Anxiety Disorders | Lymphedema-distichiasis Syndrome | Geleophysic Dysplasia | Gastroschisis | Brachial Plexus Neuropathy | Acute Lung Injury | Botulism | Hereditary Multiple Exostoses | Skin Fragility-woolly Hair Syndrome | Schnitzler Syndrome | Hypohidrotic Ectodermal Dysplasia | Carbohydrate Metabolism Disorders | Von Willebrand Disease | ICF Syndrome | Arthrogryposis | Galactosemia | Gastric Atrophy | Thrombocytopenia | Juvenile Myoclonic Epilepsy | Oligoasthenoteratozoospermia | Plasma Cell Leukemia | Spinal Muscular Atrophy | Trichorhinophalangeal Syndrome | Celiac Disease | Mannosidase Deficiency Diseases | Macular Corneal Dystrophy | Bladder Exstrophy | Long QT Syndrome Type 1 | PHARC Syndrome | MELAS Syndrome | Osteogenesis Imperfecta Type V | Nail Disorder, Nonsyndromic Congenital | Anthrax | Nephrotic Syndrome | Focal Segmental Glomerulosclerosis | Superficial Spreading Melanoma | VACTERL/VATER Association | Meesmann Corneal Dystrophy | Chromosome 8q21.11 Deletion Syndrome | HUPRA Syndrome | Kaposiform Hemangioendothelioma | Rhabdoid Tumor | Treacher Collins Syndrome | Galactosialidosis | FG Syndrome | Rett Syndrome | Pseudohypoparathyroidism Type 1A | Cholelithiasis | Pathological Gambling | Nevus | Spinocerebellar Ataxia Type 14 | Herpes Simplex Dermatitis | Porphyria Cutanea Tarda | Schaaf-Yang Syndrome | Spinocerebellar Ataxia Type 31 | Kohlschutter-Tonz Syndrome | Synovitis | Esotropia | Spinocerebellar Ataxia Type 27 | Agoraphobia | Schizoaffective Disorder | Batten Disease | Hyperlipidemia | Encephalitis, Tick-borne | Persistent Mullerian Duct Syndrome | X-linked Sideroblastic Anemia | Spinocerebellar Ataxia Type 17 | Hepatitis, Autoimmune | Lactose Intolerance | Neurofibroma, Plexiform | Malignant Fibrous Histiocytoma | Ichthyosis Hystrix, Curth-Macklin Type | Pneumonia, Bacterial | Echinococcosis | Sertoli Cell-only Syndrome | Gliosarcoma | Bullous Pemphigoid | Giant Cell Glioblastoma | Gastroenteritis | Barakat Syndrome | Menetrier Disease | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Mumps | Encephalopathy, Hepatic | Meniere's Disease | Intracerebral Hemorrhage | Familial Episodic Pain Syndrome | Astigmatism | Bietti Crystalline Dystrophy | Dermatitis Herpetiformis | Spinocerebellar Ataxia Type 1 | Ureteropelvic Junction Obstruction | Peters-plus Syndrome | PASLI Disease | X-linked Myotubular Myopathy | Renpenning Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Corticobasal Syndrome | Cerebellofaciodental Syndrome | CDKL5 Deficiency Disorder | Colorectal Adenoma | Progressive Osseous Heteroplasia | Alopecia Areata | Esophageal Carcinoma | Hemimegalencephaly | Frontometaphyseal Dysplasia | Phenylketonuria II | Centronuclear Myopathy | Primary Erythromelalgia | Diabetic Encephalopathy | Microtia | Corneal Dystrophy And Perceptive Deafness | LRBA Deficiency | Chronic Beryllium Disease | Spinocerebellar Ataxia Type 3 | Dystonia Musculorum Deformans | Acrodermatitis | Aspartylglycosaminuria | Dermatofibrosarcoma | Lipid Metabolism Disorders | Sandhoff Disease | Sclerocornea | Glycogen Storage Disease Type 0 | Obsessive-compulsive Disorder | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Congenital Primary Aphakia | Tumoral Calcinosis | Situs Inversus | Alopecia | Congenital Stationary Night Blindness | Metanephric Adenoma | WAGR Syndrome | Porphyria, Acute Intermittent | Tatton-Brown-Rahman Syndrome | Coloboma | Loeys-Dietz Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Depression | Parapsoriasis | Combined Pituitary Hormone Deficiency | Pulmonary Stenosis | Osteosclerosis | Venous Insufficiency | Postpartum Depression | Hepatitis C, Chronic | Epidermolytic Ichthyosis, Annular | LMNA-related Congenital Muscular Dystrophy | Prolymphocytic Leukemia | Chitayat Syndrome | Dentinogenesis Imperfecta | Dystonia | Vitamin D Deficiency | Cataplexy | Retinitis Pigmentosa | Renal Oncocytoma | Pyruvate Dehydrogenase Deficiency | Temporal Lobe Epilepsy | Hypercalciuria | Ophthalmoplegia | Sarcoidosis, Pulmonary | Heimler Syndrome | Glycogen Storage Disease Type 3 | Hereditary Folate Malabsorption | Roberts Syndrome | Psoriasis | Oculocutaneous Albinism | Ollier Disease | Maternally Inherited Diabetes And Deafness | Blastomycosis | Keratoacanthoma | Nephrosclerosis | Gigantism | Rhabdomyosarcoma | Peutz-Jeghers Syndrome | Spastic Paraplegia Type 7 | Pontocerebellar Hypoplasia Type 2 | Tetanus | Osteoporosis, Postmenopausal | Hydrolethalus Syndrome | Arteriosclerosis | Early Infantile Epileptic Encephalopathy 4 | X-linked Charcot-Marie-Tooth Disease | Congenital Bile Acid Synthesis Defect | Non-bullous Congenital Ichthyosiform Erythroderma | Primary Lateral Sclerosis | Charcot-Marie-Tooth Disease Type 3 | Patent Ductus Arteriosus | Inflammatory Bowel Disease | Hyperacusis | Hepatoblastoma | Sarcoidosis | Chronic Lymphocytic Leukemia | Allergic Contact Dermatitis | Hydrops Fetalis | Keratosis, Seborrheic | Borjeson-Forssman-Lehmann Syndrome | Congenital Bilateral Absence Of Vas Deferens | Hypopigmentation | Fibrosarcoma | Familial Male-limited Precocious Puberty | Corneal Edema | Hyperferritinemia-cataract Syndrome | Aphasia | Aarskog-Scott Syndrome | Long QT Syndrome Type 2 | Acute Coronary Syndrome | Hypobetalipoproteinemias | Diffuse Intrinsic Pontine Glioma | Trichothiodystrophy | Neurotoxicity | Compartment Syndrome | Glycogen Storage Disease Type 9 | Retinal Degeneration | Basal Cell Nevus Syndrome | Lysosomal Acid Lipase Deficiency | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Waardenburg Syndrome Type 2A | Alpha-thalassemia Myelodysplasia Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Osteopetrosis | Hypertension, Pulmonary | Nestor-Guillermo Progeria Syndrome | Beta-Propeller Protein-associated Neurodegeneration | Rhabdomyosarcoma, Embryonal | Mitochondrial DNA Depletion Syndrome | Familial Partial Lipodystrophy | Arteriovenous Malformations | Smith-Kingsmore Syndrome | Charcot-Marie-Tooth Disease Type 4E | Behcet's Disease | Epidermolytic Palmoplantar Keratoderma | Spinocerebellar Ataxia Type 10 | B-cell Prolymphocytic Leukemia | Myelofibrosis | Parvovirus B19 Infection | Syphilis | Pituitary Dwarfism | Paget's Disease Of The Breast | Hypocalcemia