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5C56.00 Gangliosidosis

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

synonyms

• Gangliosidosis
• GM1 gangliosidosis
• Landing disease
• GM1 gangliosidosis type 1
• Generalised gangliosidosis
• Infantile GM1 gangliosidosis
• GM1 gangliosidosis type 2
• Juvenile GM1 gangliosidosis
• GM1 gangliosidosis type 3
• Adult GM1 gangliosidosis
• GM2 gangliosidosis
• deficiency of beta-n-acetylhexosaminidase isoenzymes
• GM₂ gangliosidosis
• GM 2 gangliosidosis NOS
• Retinal dystrophy in GM2 gangliosidosis
• Sandhoff disease
• GM2 gangliosidosis type 2
• GM2 gangliosidosis 0 variant
• Hexosaminidase A and B deficiency
• Total hexosaminidase deficiency
• GM>2< gangliosidosis, type 2
• GM₂ gangliosidosis, type 2
• Infantile Sandhoff disease
• Total hexosaminidase deficiency, infantile form
• infantile GM2 gangliosidosis
• infantile GM₂ gangliosidosis
• infantile GM>2< gangliosidosis
• Juvenile Sandhoff disease
• Total hexosaminidase deficiency, juvenile form
• juvenile GM2 gangliosidosis
• juvenile GM₂ gangliosidosis
• juvenile GM>2< gangliosidosis
• Adult Sandhoff disease
• Total hexosaminidase deficiency, adult form
• adult GM2 gangliosidosis
• Tay-Sachs disease
• GM2-gangliosidosis, B, B1, AB variant
• Hexosaminidase A deficiency
• severe hexosaminidase a deficiency
• B variant of hexosaminidase A deficiency
• B variant of hexosaminidase A deficiency, infantile form
• Classic infantile acute Tay-Sachs disease
• GM2 gangliosidosis type 1
• GM₂ gangliosidosis, type 1
• GM>2< gangliosidosis, type 1
• B variant of hexosaminidase A deficiency, juvenile form
• Juvenile subacute Tay-Sachs disease
• GM2 gangliosidosis type 3
• GM₂ gangliosidosis, type 3
• GM>2< gangliosidosis, type 3
• B variant of hexosaminidase A deficiency, adult form
• Adult Tay-Sachs disease
• Chronic GM2 gangliosidosis
• B1 variant of hexosaminidase A deficiency
• Late infantile Tay-Sachs disease
• Pseudo-AB variant of hexosaminidase deficiency
• Hexosaminidase activator deficiency
• GM2 activator deficiency
• AB variant of hexosaminidase deficiency

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