Metachromatic Leukodystrophy

Informaţii despre

Nume		Metachromatic Leukodystrophy
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10		Other sphingolipidosis
Clasificare anatomică Malacards		Boli ale ochiului; Boli neuronale
Boli din aceeaşi familie		Metachromatic Leukodystrophy, Adult Form; Metachromatic Leukodystrophy, Juvenile Form; Metachromatic Leukodystrophy, Late Infantile Form

Vezi şi

Boli A-Z		Adie Pupil Adrenoleukodystrophy Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Aniridia 1 Anorexia Nervosa 1 Argininosuccinic Aciduria Arthrochalasia Ehlers-Danlos Syndrome Aspartylglucosaminuria Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Autosomal Recessive Sideroblastic Anemia Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Small Vessel Disease with or Without Ocular Anomalies Branchiootic Syndrome 1 Central Nervous System Disease Cerebral Lipidosis Cerebritis Cholecystitis Cholelithiasis Chondrodysplasia Punctata Syndrome Communicating Hydrocephalus Conduct Disorder Cone-Rod Dystrophy 2 Dementia Dystonia Early-Onset Familial Alzheimer Disease Endotheliitis Epilepsy Farber Lipogranulomatosis Fucosidosis Gangliosidosis Gm1 Gastric Dilatation Gaucher Disease, Type Iii Hashimoto Thyroiditis Hematopoietic Stem Cell Transplantation Hemihyperplasia, Isolated Hepatic Adenomas, Familial Hurler Syndrome Hydrocephalus Ichthyosis, Congenital, Autosomal Recessive 11 Ichthyosis, X-Linked Inclusion-Cell Disease Infantile Krabbe Disease Krabbe Disease Learning Disability Leukodystrophy Lipid Storage Disease Lysosomal Storage Disease Mannosidosis Metabolic Acidosis Metachromatic Leukodystrophy, Adult Form Metachromatic Leukodystrophy Due to Saposin B Deficiency Metachromatic Leukodystrophy, Juvenile Form Metachromatic Leukodystrophy, Late Infantile Form Mucolipidosis Ii Alpha/beta Mucolipidosis Iv Mucopolysaccharidosis Iii Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Ii Mucopolysaccharidosis Type Vi Multiple Sclerosis Multiple Sulfatase Deficiency Nervous System Disease Neuronitis Neuropathy Phelan-Mcdermid Syndrome Polyneuropathy Pseudoarylsulfatase a Deficiency Quadriplegia Renal Tubular Acidosis Schizophrenia Scott Syndrome Spasticity Spastic Quadriplegia Sphingolipidosis Spondylocarpotarsal Synostosis Syndrome Tay-Sachs Disease Thyroiditis Tremor Tuberous Sclerosis Tuberous Sclerosis 1 Undifferentiated Pleomorphic Sarcoma X-Linked Chondrodysplasia Punctata Yemenite Deaf-Blind Hypopigmentation Syndrome