Sialidosis Type I

About the Disease
Neuraminidase Deficiency, also known as lipomucopolysaccharidosis, is related to neu-laxova syndrome 1 and galactosialidosis. An important gene associated with Neuraminidase Deficiency is NEU1 (Neuraminidase 1). The drug polysaccharide-K has been mentioned in the context of this disorder. Affiliated tissues include bone marrow, bone and eye, and related phenotypes are neurological speech impairment and scoliosis

Common Targets
NEU1 | UGCG

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Hyperparathyroidism, Secondary | Sponastrime Dysplasia | Endophthalmitis | Homocystinuria | Obsessive-compulsive Disorder | Chronic Granulomatous Disease, X-linked | Cohen Syndrome | Dominant Optic Atrophy | AIDS | Hypertriglyceridemia | Lipodystrophy | Hypersensitivity Pneumonitis | Heart Septal Defects | Infertility | Xeroderma Pigmentosum | Agammaglobulinemia | Ectopia Lentis, Isolated, Autosomal Recessive | Esophagitis, Eosinophilic | Myofibrillar Myopathy | Cerebrotendinous Xanthomatosis | Craniofrontonasal Syndrome | Limb Girdle Muscular Dystrophy | Congenital Afibrinogenemia | Hypercalciuria | Angiosarcoma | Epidermolysis Bullosa Simplex, Localized | Glutaric Aciduria Type 2 | Cerebral Cavernous Malformations | Chordoma | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Usher Syndrome Type III | Hyperthyroidism | Li-Fraumeni Syndrome | Polyneuropathy | Thyrotoxic Periodic Paralysis | Sialoadenitis | Sulfite Oxidase Deficiency | Keloid | Multiple Mitochondrial 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Autoimmune Disease | Spinocerebellar Ataxia Type 10 | Keratosis, Seborrheic | Waardenburg Syndrome Type 2A | Blomstrand Osteochondrodysplasia | Bardet-Biedl Syndrome | Obesity | Rosacea | Spinocerebellar Ataxia Type 23 | Stargardt Disease | Juvenile Xanthogranuloma | Acrodysostosis | Spinocerebellar Ataxia | Hartsfield Syndrome | Spitzoid Melanoma | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Deafness, Dystonia, And Cerebral Hypomyelination | Rhinitis | Cardiac Arrest | Epilepsy | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Gaucher Disease | Heterotopic Ossification | Extramammary Paget's Disease | Crisponi Syndrome | Astrocytoma | Central Pain Syndrome | Brenner Tumor | Molybdenum Cofactor Deficiency | Stomatitis | Anti-glomerular Basement Membrane Disease | Mycosis Fungoides | Neurotoxicity | Facioscapulohumeral Muscular Dystrophy Type 1 | Olmsted Syndrome | Cramp Fasciculation Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | 3-hydroxy-3-methylglutaric 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