5C56.00
category
Gangliosidosis
Also indexed as
AB variant of hexosaminidase deficiencyAdult GM1 gangliosidosisAdult Sandhoff diseaseAdult Tay-Sachs diseaseB variant of hexosaminidase A deficiencyB variant of hexosaminidase A deficiency, adult formB variant of hexosaminidase A deficiency, infantile formB variant of hexosaminidase A deficiency, juvenile formB1 variant of hexosaminidase A deficiencyChronic GM2 gangliosidosisClassic infantile acute Tay-Sachs diseaseGM 2 gangliosidosis NOSGM1 gangliosidosisGM1 gangliosidosis type 1GM1 gangliosidosis type 2GM1 gangliosidosis type 3GM2 activator deficiencyGM2 gangliosidosisGM2 gangliosidosis 0 variantGM2 gangliosidosis type 1GM2 gangliosidosis type 2GM2 gangliosidosis type 3GM2-gangliosidosis, B, B1, AB variantGM2 gangliosidosisGM2 gangliosidosis, type 1GM2 gangliosidosis, type 2GM2 gangliosidosis, type 3GM>2< gangliosidosis, type 1GM>2< gangliosidosis, type 2GM>2< gangliosidosis, type 3GangliosidosisGeneralised gangliosidosisHexosaminidase A and B deficiencyHexosaminidase A deficiencyHexosaminidase activator deficiencyInfantile GM1 gangliosidosisInfantile Sandhoff diseaseJuvenile GM1 gangliosidosisJuvenile Sandhoff diseaseJuvenile subacute Tay-Sachs diseaseLanding diseaseLate infantile Tay-Sachs diseasePseudo-AB variant of hexosaminidase deficiencyRetinal dystrophy in GM2 gangliosidosisSandhoff diseaseTay-Sachs diseaseTotal hexosaminidase deficiencyTotal hexosaminidase deficiency, adult formTotal hexosaminidase deficiency, infantile formTotal hexosaminidase deficiency, juvenile formadult GM2 gangliosidosisdeficiency of beta-n-acetylhexosaminidase isoenzymesinfantile GM2 gangliosidosisinfantile GM2 gangliosidosis Type 2infantile GM2 gangliosidosis, type IIjuvenile GM2 gangliosidosisjuvenile GM2 gangliosidosisjuvenile GM>2< gangliosidosissevere hexosaminidase a deficiency