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unspecified gangliosidosis

Medical Definition

Group of often fatal inherited diseases marked by the accumulation of gangliosides in lysosomes secondary to enzymatic deficiency states; gangliosidoses include tay-sachs disease, gangliosidosis gm1, gangliosidoses gm2, and sandhoff disease; which share the infantile or childhood onset of central nervous system deterioration.
Related Codes (1)
Code
Description
Billable
Details
E75.10Unspecified gangliosidosis

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