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Diagnosis Code

E75.22 GAUCHER DISEASE


Code Information

Diagnosis Code: E75.22

Short Description: Gaucher disease

Long Description: Gaucher disease

The code E75.22 is VALID for claim submission

Code Classification:

  • Endocrine, nutritional and metabolic diseases (E00–E89)
    • Metabolic disorders (E70-E88)
      • Disord of sphingolipid metab and oth lipid storage disorders (E75)
        • E75.22 Gaucher disease

Code Version: 2022 ICD-10-CM


Synonyms

  • Acute neuronopathic Gaucher's disease
  • Atypical Gaucher disease due to saposin C deficiency
  • Cerebral degeneration in Gaucher's disease
  • Chronic non-neuropathic Gaucher's disease
  • Gaucher disease with ophthalmoplegia and cardiovascular calcification
  • Gaucher's disease
  • Gaucher's disease
  • Kerasin thesaurismosis
  • Perinatal lethal Gaucher disease
  • Subacute neuronopathic Gaucher's disease
  • Subacute neuronopathic Gaucher's disease

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
E75.22 Right Arrow 272.7 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
E75.23 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
E75.4 Neuronal ceroid lipofuscinosis
E75.5 Other lipid storage disorders
E75.6 Lipid storage disorder, unspecified

This page was last updated on: 10/1/2023

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