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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Synpolydactyly | Sleep Apnea | Ghosal Syndrome | Gastroenteritis, Eosinophilic | Congenital Bile Acid Synthesis Defect | Anorexia Nervosa | Neurodermatitis | Sandhoff Disease | Syndactyly | Cholangiocarcinoma | Diarrhea | Spondylosis | Neuromyotonia | Epithelioid Hemangioma | Trichorhinophalangeal Syndrome | Chondromyxoid Fibroma | Thrombophilia | Pre-eclampsia | Vitamin A Deficiency | Ebstein Anomaly | Cysticercosis | Osteoglophonic Dysplasia | Lymphangioleiomyomatosis | GAPO Syndrome | Microtia | Pneumococcal Meningitis | Prediabetes | Uremia | Autosomal Recessive Spastic Paraplegia Type 35 | Placenta Previa | Ellis-Van Creveld Syndrome | Ganglioneuroma | HIBCH Deficiency | Analgesia | Osteoporosis-pseudoglioma Syndrome | Anorchia | Hypersensitivity Pneumonitis | Pulmonary Capillary Hemangiomatosis | Microcephaly, Seizures, And Developmental Delay | Hereditary Sensory Neuropathy Type 1 | Juvenile Myelomonocytic Leukemia | Kidney Stones | Hypersensitivity | Protein C Deficiency | Spinocerebellar Ataxia Type 8 | Leukemia | Persistent Hyperplastic Primary Vitreous | Bulimia Nervosa | Polyomavirus Nephropathy | Thyroid Dyshormonogenesis | Dental Caries | Blau Syndrome | Neurodegeneration With Brain Iron Accumulation | Acute Kidney Injury | Robinow Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Argininosuccinic Aciduria | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | AIDS | Congenital Stationary Night Blindness | Papilledema | Pontocerebellar Hypoplasia Type 7 | Sick Sinus Syndrome 1 | Niemann-Pick Disease, Type A | Autism | Stroke, Ischemic | Cranial Nerve Disease | Restrictive Dermopathy | Long QT Syndrome Type 3 | Leishmaniasis, Cutaneous | Autosomal Recessive Bestrophinopathy | Acrodermatitis | Multiple Sclerosis | Mitochondrial Disease | Acute Myeloid Leukemia | Hidradenitis Suppurativa | Lichen Sclerosus | Pseudohermaphroditism | Neurofibromatosis Type 1 | Trichuriasis | Focal Facial Dermal Dysplasia | Tatton-Brown-Rahman Syndrome | Hypertension, Renal | Megaloblastic Anemia | Encephalopathy, Ethylmalonic | Larsen Syndrome | H Syndrome | Jawad Syndrome | Plasma Cell Dyscrasia | Pregnancy, Ectopic | Sporadic Inclusion Body Myositis | Partington Syndrome | Torticollis | Amyotrophic Lateral Sclerosis, Juvenile | Cryptorchidism | Raynaud Phenomenon | Acute Coronary Syndrome | Motion Sickness | Spinocerebellar Ataxia Type 12 | Methylmalonic Acidemia | Hereditary Neuropathy With Liability To Pressure Palsies | Seborrheic Dermatitis | Dowling-Degos Disease | Cirrhosis | Myoclonic Epilepsy With Ragged Red Fibers | Auriculocondylar Syndrome | Glucagonoma | Brenner Tumor | Congenital Hypofibrinogenemia | Spinocerebellar Ataxia Type 15 | Pulmonary Tuberculosis | Amenorrhea | Ophthalmia, Sympathetic | Transient Bullous Dermolysis Of The Newborn | Keratopathy | Tibial Muscular Dystrophy | Intracerebral Hemorrhage | Chloridorrhea, Congenital | Chronic Idiopathic Myelofibrosis | Craniofrontonasal Syndrome | Myocardial Infarction 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Thanatophoric Dysplasia Type 1 | Premature Ejaculation | Vitreoretinopathy, Proliferative | Retinal Coloboma | Sarcomatoid Carcinoma Of The Lung | Angioimmunoblastic T-cell Lymphoma | Aplasia Cutis Congenita | Pleomorphic Xanthoastrocytoma | Xeroderma Pigmentosum Variant Type | Woodhouse-Sakati Syndrome | Central Retinal Artery Occlusion | Anovulation | Thrombophlebitis | Cutis Laxa | Pantothenate Kinase-associated Neurodegeneration | Dentinogenesis Imperfecta | Glycogen Storage Disease Type 9 | Focal Dermal Hypoplasia | Peyronie's Disease | Seasonal Mood Disorder | Dysfibrinogenemia | Marshall-Smith Syndrome | Nanophthalmos | Genitopatellar Syndrome | Psoriasis | Osteogenesis Imperfecta Type II | Poirier-Bienvenu Neurodevelopmental Syndrome | Sclerocornea | Aphasia | Angiomyolipoma | Thyroid Hormone Resistance | Chronic Myeloid Leukemia | Melanoma, Uveal | Bladder Exstrophy | Erectile Dysfunction | Spasticity | Anorectal Malformations | Warsaw Breakage Syndrome | Glaucoma | Cerebellar 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