E75.10

Applicable To

• Gangliosidosis NOS

Approximate Synonyms

• Gangliosidosis

Clinical Information

• A group of autosomal recessive lysosomal storage disorders marked by the accumulation of gangliosides. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the lysosomes. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.

• 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.

Details

• E75.10 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM E75.10 became effective on October 1, 2022.

• This is the American ICD-10-CM version of E75.10 – other international versions of ICD-10 E75.10 may differ.