5C56.00
Gangliosidosis
Gangliosidose
CategoryIndex Terms
GangliosidosisGM1 gangliosidosisLanding diseaseGM1 gangliosidosis type 1Generalised gangliosidosisInfantile GM1 gangliosidosisGM1 gangliosidosis type 2Juvenile GM1 gangliosidosisGM1 gangliosidosis type 3Adult GM1 gangliosidosisGM2 gangliosidosisdeficiency of beta-n-acetylhexosaminidase isoenzymesGM2 gangliosidosisGM 2 gangliosidosis NOSRetinal dystrophy in GM2 gangliosidosisSandhoff diseaseGM2 gangliosidosis type 2GM2 gangliosidosis 0 variantHexosaminidase A and B deficiencyTotal hexosaminidase deficiencyGM>2< gangliosidosis, type 2GM2 gangliosidosis, type 2Infantile Sandhoff diseaseTotal hexosaminidase deficiency, infantile forminfantile GM2 gangliosidosisinfantile GM2 gangliosidosisinfantile GM>2< gangliosidosisJuvenile Sandhoff diseaseTotal hexosaminidase deficiency, juvenile formjuvenile GM2 gangliosidosisjuvenile GM2 gangliosidosisjuvenile GM>2< gangliosidosisAdult Sandhoff diseaseTotal hexosaminidase deficiency, adult formadult GM2 gangliosidosisTay-Sachs diseaseGM2-gangliosidosis, B, B1, AB variantHexosaminidase A deficiencysevere hexosaminidase a deficiencyB variant of hexosaminidase A deficiencyB variant of hexosaminidase A deficiency, infantile formClassic infantile acute Tay-Sachs diseaseGM2 gangliosidosis type 1GM2 gangliosidosis, type 1GM>2< gangliosidosis, type 1B variant of hexosaminidase A deficiency, juvenile formJuvenile subacute Tay-Sachs diseaseGM2 gangliosidosis type 3GM2 gangliosidosis, type 3GM>2< gangliosidosis, type 3B variant of hexosaminidase A deficiency, adult formAdult Tay-Sachs diseaseChronic GM2 gangliosidosisB1 variant of hexosaminidase A deficiencyLate infantile Tay-Sachs diseasePseudo-AB variant of hexosaminidase deficiencyHexosaminidase activator deficiencyGM2 activator deficiencyAB variant of hexosaminidase deficiency