Disease

Multiple Sulfatase Deficiency

About the Disease
Multiple Sulfatase Deficiency, also known as mucosulfatidosis, is related to leukodystrophy and ichthyosis, x-linked, and has symptoms including ataxia and muscle spasticity. An important gene associated with Multiple Sulfatase Deficiency is SUMF1 (Sulfatase Modifying Factor 1), and among its related pathways/superpathways are Metabolism and Glycosaminoglycan metabolism. Affiliated tissues include skin, bone and eye, and related phenotypes are intellectual disability and developmental regression

Common Targets
SUMF1

疾病靶点研报
Multiple Sulfatase Deficiency

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

Other Diseases

Rhabdoid Tumor | Poretti-Boltshauser Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Anovulation | Sweet Syndrome | Bipolar Disorder | Keratopathy | Aneurysm, Thoracic Aortic | Precocious Puberty | Acute Coronary Syndrome | Brugada Syndrome 1 | ACTH-independent Macronodular Adrenal Hyperplasia | Hemorrhagic Disorders | Periventricular Leukomalacia | Cysticercosis | Ocular Hypertension | Menkes Disease | Cabezas Syndrome | Corneal Dystrophy | Progressive Encephalopathy-optic Atrophy Syndrome | IgA Deficiency | Blepharitis | Antisynthetase Syndrome | Benign Hereditary Chorea | Light Chain Amyloidosis | VEXAS Syndrome | Multiple Sclerosis, Chronic Progressive | Lymphangioleiomyomatosis | Sarcoma | Galactosemia | Keratosis, Actinic | Acute Kidney Injury | Microcephalic Primordial Dwarfism | Noonan Syndrome | Leiomyosarcoma | Necrobiosis Lipoidica | Iron Metabolism Disorders | Depression | Familial Advanced Sleep Phase Syndrome | Specific Granule Deficiency | Cholestasis, Intrahepatic | Gout | Oculocutaneous Albinism Type 2 | Fraser Syndrome | Pre-eclampsia | Diabetes Insipidus, Neurogenic | Spinal And Bulbar Muscular Atrophy | Asplenia | Patent Foramen Ovale | Oligoastrocytoma | Dengue Hemorrhagic Fever | Macrodactyly | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Dystrophy, Cone-rod | Glycogen Storage Disease Type 0, Muscle | Generalized Epilepsy And Paroxysmal Dyskinesia | Wilson's Disease | Peripheral T-cell Lymphoma | PHARC Syndrome | Proopiomelanocortin Deficiency | Metachromatic Leukodystrophy | Chordoid Glioma | Vascular Cognitive Impairment | Infantile Spasm | Heterotaxy | Small Lymphocytic Lymphoma | Dermatitis Herpetiformis | Prolactinoma | Trichomegaly | Primary Familial Brain Calcification | Hypertension, Renal | Granular Corneal Dystrophy | Yellow Fever | Hypotension, Orthostatic | Acne Vulgaris | Focal Facial Dermal Dysplasia | Diffuse Intrinsic Pontine Glioma | Corneal Dystrophy And Perceptive Deafness | Hartsfield Syndrome | Anal Fissure | Birt-Hogg-Dube Syndrome | Diabetic Neuropathy | Hermansky-Pudlak Syndrome | Chronic Idiopathic Myelofibrosis | Alpha-thalassemia Myelodysplasia Syndrome | Peritonitis | Vitelliform Macular Dystrophy | Pyruvate Carboxylase Deficiency Disease | Takayasu's Arteritis | Conjunctivitis, Allergic | Osteoarthritis | Giant Cell Glioblastoma | Greenberg Dysplasia | Transient Bullous Dermolysis Of The Newborn | Bicuspid Aortic Valve | Pyruvate Dehydrogenase Deficiency | Sporadic Hemiplegic Migraine | Spinal Cord Diseases | Hydrolethalus Syndrome | Glycogen Storage Disease Type 1a | Aplastic Anemia | Central Core Disease | Pulmonary Tuberculosis | Persistent Mullerian Duct Syndrome | GNE Myopathy | Shprintzen-Goldberg Syndrome | Leukoencephalopathy, Progressive Multifocal | Adenoid Cystic Carcinoma | Non-epidermolytic Palmoplantar Keratoderma | Tay-Sachs Disease | Incontinentia Pigmenti | Lipid Metabolism Disorders | Acute Motor Axonal Neuropathy | Osteogenesis Imperfecta Type I | Pendred Syndrome | Huntington's Disease | Paroxysmal Kinesigenic Dyskinesia | Spondylometaphyseal Dysplasia | Usher Syndrome Type I | Melanoma, Malignant | Antiphospholipid Syndrome | Basal Ganglia Cerebrovascular Disease | Vitreoretinopathy, Proliferative | Myelitis, Transverse | Erythromelalgia | Neurofibromatosis Type 1 | Anti-glomerular Basement Membrane Disease | Primary Aldosteronism | Von Hippel-Lindau Disease | Ovarian Sex Cord-stromal Tumor | Hydronephrosis | Tremor | Currarino Syndrome | Smith-Magenis Syndrome | Lymphoma, B-cell | Guanidinoacetate Methyltransferase Deficiency | Sjogren Syndrome | Acute Lymphocytic Leukemia | Carcinoma, Transitional Cell | Abetalipoproteinemia | Stroke, Hemorrhagic | Acrodysostosis | Keratosis | Turner's Syndrome | Optic Nerve Hypoplasia, Bilateral | CREST Syndrome | Compartment Syndrome | Okihiro Syndrome | Blue Nevus | Trichotillomania | Niemann-Pick Disease, Type A | Fanconi Anemia | Alopecia | Cold-induced Sweating Syndrome | Paraganglioma, Carotid Body | Ellis-Van Creveld Syndrome | Multiple Hamartoma Syndrome | Cutaneous T-cell Lymphoma | Saethre-Chotzen Syndrome | Tyrosinemia Type 1 | Barrett Esophagus | Optic Neuritis | Neural Tube Defect | Meningitis | Primary Progressive Aphasia | Heimler Syndrome | Neurodegeneration With Brain Iron Accumulation | Goldenhar Syndrome | Diabetic Nephropathy | Addison Disease | Fetal Akinesia Deformation Sequence | Senior-Loken Syndrome | Pneumococcal Meningitis | Oligodendroglioma | Diabetic Macular Edema | Extramammary Paget's Disease | Corneal Ulcer | Infantile Refsum Disease | Hepatic Veno-occlusive Disease | Polycystic Ovary Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Schwartz-Jampel-Aberfeld Syndrome | Bruck Syndrome | Vulvovaginitis | Liddle Syndrome | Nephrotic Syndrome | Hypogammaglobulinemia | Osteosclerosis | Scapuloperoneal Myopathy, X-linked Dominant | Scoliosis | Osteoporosis, Postmenopausal | Nicotine Addiction | HIBCH Deficiency | Vertebrobasilar Insufficiency | Lyme Disease | Pyruvate Decarboxylase Deficiency | Guttate Psoriasis | Lathosterolosis | Focal Cortical Dysplasia Type 2 | Intestinal Pseudo-obstruction | Spinocerebellar Ataxia Type 1 | Gilbert Syndrome | Neurofibromatosis-Noonan Syndrome | Atherosclerosis | Prune Belly Syndrome | Familial Cerebral Amyloid Angiopathy | Congenital Myasthenic Syndrome | Protein S Deficiency | Vitiligo | Influenza | Charcot-Marie-Tooth Disease Type 2E | Leukemia | Congenital Ichthyosiform Erythroderma | Cannabis Abuse | Glioblastoma | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Nephritis, Interstitial | Spinocerebellar Ataxia Type 21 | Cherubism | Inflammatory Bowel Disease | Proteus Syndrome | Neurogenic Bladder | Postpoliomyelitis Syndrome | Peroxisomal Disorder | Juvenile Myelomonocytic Leukemia | Deafness, Dystonia, And Cerebral Hypomyelination | Glycogen Storage Disease Type 4 | Adenoma, Pleomorphic | Pulmonary Capillary Hemangiomatosis | Cutis Laxa | Skin Carcinoma | Fabry's Disease | HUPRA Syndrome | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Leber Hereditary Optic Neuropathy | Acute Myeloid Leukemia | Glycogen Storage Disease Type 6 | Analgesia | Osteopetrosis | Disseminated Superficial Actinic Porokeratosis | Methemoglobinemia Type IV | Charcot-Marie-Tooth Disease Type 2D | Choroiditis | Diamond-Blackfan Anemia | Hyperlipidemia, Familial Combined | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Tangier Disease | Heart Failure | Heroin Dependence | Congenital Tufting Enteropathy | Nemaline Myopathy 10 | Sick Sinus Syndrome 1 | Cerebellofaciodental Syndrome | Paget's Disease Of The Breast | Renal Hypouricemia | Spermatocele | Lesch-Nyhan Syndrome | Polydactyly | Alpha-1 Antitrypsin Deficiency | Charcot-Marie-Tooth Disease, Type 2A | Nevus | Meningioma, Benign | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Hyperacusis | Camurati-Engelmann Disease | McLeod Syndrome | Multiple Sclerosis | Blastoma, Pleuropulmonary | Pitt-Hopkins Syndrome | Whipple's Disease | Spinocerebellar Ataxia Type 2 | Celiac Disease | Chondromyxoid Fibroma | Wolman Disease | Acromegaly | 3-methylglutaconic Aciduria | Brooke-Spiegler Syndrome | Sleep Disorder | Keratocystic Odontogenic Tumor | Neurocysticercosis | Cerebrotendinous Xanthomatosis | Postpartum Depression | Osteonecrosis | Myositis, Focal | Spastic Paraplegia Type 7 | L-2-Hydroxyglutaric Aciduria | CDKL5 Deficiency Disorder | Chromosome 5q Deletion Syndrome | GATA2 Deficiency | Epidermolysis Bullosa Simplex, Generalized | Benign Familial Pemphigus | N-acetylglutamate Synthase Deficiency | Sleep Apnea | Cholangiocarcinoma | Mohr-Tranebjaerg Syndrome | Brachydactyly | Hyperlipidemia Type V | Leishmaniasis, Cutaneous | Malignant Peripheral Nerve Sheath Tumor | Corneal Dystrophies, Hereditary | Cutaneous Mastocytosis | Richter's Syndrome | Hypercholesterolemia, Familial | Hemorrhage | Oculocutaneous Albinism | Erythema Multiforme | Waardenburg Syndrome Type 2A | Congenital Dyserythropoietic Anemia | Japanese Encephalitis | Craniofrontonasal Syndrome | Endometritis | Retinal Detachment | Sengers Syndrome | TARP Syndrome | Pityriasis Rubra Pilaris | Insulin Resistance | Chronic Beryllium Disease | Spinal Muscular Atrophy | Charcot-Marie-Tooth Disease Type 2T | Cardiospondylocarpofacial Syndrome | Zollinger-Ellison Syndrome | Colorectal Adenoma | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Lymphopenia | Myopathy | Mitochondrial Encephalomyopathy | Ornithine Transcarbamylase Deficiency | Leigh Syndrome | Adenosine Deaminase Deficiency | Retinal Dystrophy | Neonatal Progeroid Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Keratoconjunctivitis | Conn Syndrome | Dermatomyositis | McCune-Albright Syndrome | Alopecia Areata | Pancreatitis | Heavy Chain Disease | Chiari Malformation Type I | Osteomalacia | Tatton-Brown-Rahman Syndrome | Pituitary Stalk Interruption Syndrome | Purpura, Thrombotic Thrombocytopenic | Mannosidase Deficiency Diseases | Reticular Dysgenesis | Hereditary Pyropoikilocytosis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Chronic Periodontitis | Weill-Marchesani Syndrome | Encephalitis | Osteogenesis Imperfecta Type VI | Synovitis | Congenital Bile Acid Synthesis Defect | Dengue Shock Syndrome | KBG Syndrome | Asthma, Exercise-induced | Spinocerebellar Ataxia Type 6 | Scleroderma, Diffuse | Carpenter Syndrome | Eosinophilia | Spinocerebellar Ataxia Type 27 | Waardenburg Syndrome Type 4 | Benign Recurrent Intrahepatic Cholestasis 1 | Mitochondrial DNA Depletion Syndrome | Retinoblastoma | Tibial Muscular Dystrophy | Myeloid Leukemia | Amblyopia | Fibrodysplasia Ossificans Progressiva | Ligneous Conjunctivitis | X-linked Sideroblastic Anemia | Multifocal Motor Neuropathy | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Hypertelorism | Hypoglycemia | Asthma | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Fucosidosis | Pseudohypoparathyroidism Type 1A | Papulopustular Rosacea | LMNA-related Congenital Muscular Dystrophy | Cancer, Brain | Usher Syndrome Type II | Prolidase Deficiency | Hepatitis D | Mosaic Variegated Aneuploidy Syndrome 2 | Meesmann Corneal Dystrophy | Intellectual Disability, Autosomal Dominant 5 | Astigmatism | Sensory Neuropathy | Pleural Tuberculosis | Short-chain Acyl-CoA Dehydrogenase Deficiency | Pure Red Cell Aplasia | Takotsubo Cardiomyopathy | Periodontitis | Benign Familial Infantile Seizures | Myotonia | Heart Septal Defects | Hypermetropia