Diagnosis Code: E75.29

Short Description: Other sphingolipidosis

Long Description: Other sphingolipidosis

The code E75.29 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)
      • E75.29 Other sphingolipidosis

Code Version: 2022 ICD-10-CM

Synonyms

• 4H leukodystrophy
• 4H leukodystrophy
• Adult onset autosomal dominant leukodystrophy
• Alkaline ceramidase 3 deficiency
• C11ORF73-related autosomal recessive hypomyelinating leukodystrophy
• Combined malformation of central nervous system and skeletal muscle
• Deficiency of arylsulfatase
• Deficiency of cerebroside-sulfatase
• Deficiency of N-acetylgalactosamine-6-sulfatase
• Deficiency of placental function
• Deficiency of steryl-sulfatase
• Deficiency of steryl-sulfatase
• Deficiency of steryl-sulfatase
• Dementia due to leukodystrophy
• Disorder of placental endocrine function
• Encephalopathy due to prosaposin deficiency
• Galactosylceramide lipidosis
• Hereditary cerebellar atrophy
• Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum
• Leukodystrophy
• Metachromatic leukodystrophy
• Metachromatic leukodystrophy due to sphingolipid activator protein I deficiency
• Multiple sulfatase deficiency
• Muscle eye brain disease with bilateral multicystic leukodystrophy
• Neuroaxonal dystrophy
• Neuroaxonal leukodystrophy
• NKX6-2-related autosomal recessive hypomyelinating leukodystrophy
• Non-progressive predominantly posterior cavitating leukodystrophy with peripheral neuropathy
• Odontoleukodystrophy
• Ovarioleukodystrophy
• Pelizaeus Merzbacher like disease
• Pelizaeus Merzbacher like disease
• Pelizaeus Merzbacher like disease
• Pelizaeus Merzbacher like disease
• Pelizaeus Merzbacher like disease due to AIMP1 mutation
• Pelizaeus Merzbacher like disease due to GJC2 mutation
• Pelizaeus Merzbacher like disease due to HSPD1 mutation
• Pelizaeus Merzbacher like disease due to SLC16A2 mutation
• Pelizaeus-Merzbacher disease
• Pelizaeus-Merzbacher disease in female carrier
• Pelizaeus-Merzbacher disease null syndrome
• Pelizaeus-Merzbacher disease, classic form
• Pelizaeus-Merzbacher disease, connatal variant
• Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
• Placental sulfatase deficiency
• Premature ovarian failure
• RARS-related autosomal recessive hypomyelinating leukodystrophy
• RNA polymerase III-related leukodystrophy
• Spastic tetraplegia
• Spongy degeneration of central nervous system
• TUBB4A-related leukodystrophy
• TUBB4A-related leukodystrophy
• Type III transitional Pelizaeus-Merzbacher disease
• Type IV adult Pelizaeus-Merzbacher disease
• Type V atypical Pelizaeus-Merzbacher disease
• Type VI Cockayne Pelizaeus-Merzbacher disease
• Vanishing white matter disease
• VPS11-related autosomal recessive hypomyelinating leukodystrophy
• Waardenburg syndrome
• X-linked ichthyosis with steryl-sulfatase deficiency

References to Index of Diseases and Injuries

The code E75.29 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Farber's syndrome
  • Sulfatide lipidosis

Crosswalk Information

Similar Codes

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

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