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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