Ganglioside sialidase deficiency
An autosomal recessive lysosomal storage disease caused by mutations in the mcoln1 gene. It is characterized by psychomotor developmental delays and ophthalmologic abnormalities.
E75.11 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 E75.11 became effective on October 1, 2022.
This is the American ICD-10-CM version of E75.11 – other international versions of ICD-10 E75.11 may differ.