Informaţii despre

Nume Tay-Sachs Disease
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 GM2 gangliosidosis
Clasificare anatomică Malacards Boli ale ochiului; Boli neuronale
Boli din aceeaşi familie Tay-Sachs Disease, B Variant, Adult Form; Tay-Sachs Disease, B Variant, Infantile Form; Tay-Sachs Disease, B Variant, Juvenile Form; Tay-Sachs Disease, B1 Variant

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Achalasia Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Autosomal Recessive Disease Autosomal Recessive Sideroblastic Anemia Beta-Thalassemia Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Branchiootic Syndrome 1 Cerebral Lipidosis Cerebritis Choroiditis Chromosomal Triplication Constricting Bands, Congenital Cystic Fibrosis Dementia Encephalitis Fabry Disease Fucosidosis Galactosialidosis Gangliosidosis Gm1 Gangliosidosis Gm2 Glycoproteinosis Gm2-Gangliosidosis, Ab Variant Hepatic Adenomas, Familial Hexosaminidase C Inclusion-Cell Disease Juvenile Spinal Muscular Atrophy Krabbe Disease Leukodystrophy Lipid Metabolism Disorder Lipid Storage Disease Lipodystrophy Lysosomal Storage Disease Mannosidosis, Alpha B, Lysosomal Mannosidosis, Beta a, Lysosomal Metachromatic Leukodystrophy Metachromatic Leukodystrophy, Adult Form Metachromatic Leukodystrophy, Juvenile Form Metachromatic Leukodystrophy, Late Infantile Form Mucolipidosis Ii Alpha/beta Mucolipidosis Iv Mucopolysaccharidosis Iv Myoclonic Cerebellar Dyssynergia Neuronitis Neuropathy Niemann-Pick Disease Phenylketonuria Pick Disease of Brain Polyglucosan Body Myopathy 1 with or Without Immunodeficiency Prader-Willi Syndrome Precocious Puberty Ptosis Retinitis Sandhoff Disease Scheie Syndrome Schizophrenia Sickle Cell Disease Sphingolipidosis Stuttering Tay-Sachs Disease, B1 Variant Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thrombocytopenia Undifferentiated Pleomorphic Sarcoma Yemenite Deaf-Blind Hypopigmentation Syndrome