E75.4 NEURONAL CEROID LIPOFUSCINOSIS

Code Information

  • Diagnosis Code: E75.4
  • Short Description: Neuronal ceroid lipofuscinosis
  • Long Description: Neuronal ceroid lipofuscinosis
  • Code Version: 2025 ICD-10-CM

The code E75.4 is VALID for claim submission

Code Classification

Synonyms

  • Acquired ataxia
  • Adult neuronal ceroid lipofuscinosis
  • ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis
  • Cerebral degeneration in childhood
  • Cerebral lipidosis
  • Congenital neuronal ceroid lipofuscinosis
  • Dementia associated with cerebral lipidosis
  • Infantile neuronal ceroid lipofuscinosis
  • Juvenile neuronal ceroid lipofuscinosis
  • Late-infantile neuronal ceroid lipofuscinosis
  • Myoclonic disorder due to neuronal ceroid lipofuscinosis
  • Neuronal ceroid lipofuscinosis
  • Neuronal ceroid lipofuscinosis 8
  • Neuronal ceroid lipofuscinosis type 6A

References to Index of Diseases and Injuries

The code E75.4 has the following ICD-10-CM references to the Index of Diseases and Injuries

  • Inclusion Terms:
    • Batten disease
    • Bielschowsky-Jansky disease
    • Kufs disease
    • Spielmeyer-Vogt disease

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
E75.4 Right Arrow 330.1 Cerebral lipidoses
This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
E75 Disorders of sphingolipid metabolism and other lipid storage disorders
E75.0 GM2 gangliosidosis
E75.00 GM2 gangliosidosis, unspecified
E75.01 Sandhoff disease
E75.02 Tay-Sachs disease
E75.09 Other GM2 gangliosidosis
E75.1 Other and unspecified gangliosidosis
E75.10 Unspecified gangliosidosis
E75.11 Mucolipidosis IV
E75.19 Other gangliosidosis
E75.2 Other sphingolipidosis
E75.21 Fabry (-Anderson) disease
E75.22 Gaucher disease
E75.23 Krabbe disease
E75.24 Niemann-Pick disease
E75.240 Niemann-Pick disease type A
E75.241 Niemann-Pick disease type B
E75.242 Niemann-Pick disease type C
E75.243 Niemann-Pick disease type D
E75.244 Niemann-Pick disease type A/B
E75.248 Other Niemann-Pick disease
E75.249 Niemann-Pick disease, unspecified
E75.25 Metachromatic leukodystrophy
E75.26 Sulfatase deficiency
E75.27 Pelizaeus-Merzbacher disease
E75.28 Canavan disease
E75.29 Other sphingolipidosis
E75.3 Sphingolipidosis, unspecified
E75.5 Other lipid storage disorders
E75.6 Lipid storage disorder, unspecified
This page was last updated on: 10/1/2024
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