ICD-10-CM Codes
E00-E89
E70-E88
Disorders of sphingolipid metabolism and other lipid storage disorders E75

Disorders of sphingolipid metabolism and other lipid storage disorders E75-

Type 1 Excludes

Type 1 Excludes Help

A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as E75. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

mucolipidosis, types I-III (
ICD-10-CM Diagnosis Code E77.0
Defects in post-translational modification of lysosomal enzymes
Applicable To
- Mucolipidosis II [I-cell disease]
- Mucolipidosis III [pseudo-Hurler polydystrophy]
E77.0-
ICD-10-CM Diagnosis Code E77.1
Defects in glycoprotein degradation
Applicable To
- Aspartylglucosaminuria
- Fucosidosis
- Mannosidosis
- Sialidosis [mucolipidosis I]
E77.1
)
Refsum's disease (
ICD-10-CM Diagnosis Code G60.1
Refsum's disease
Applicable To
- Infantile Refsum disease
G60.1
)

Codes

E75 Disorders of sphingolipid metabolism and other lipid storage disorders
- E75.0 GM2 gangliosidosis
  - E75.00 …… 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 …… type A
    - E75.241 …… type B
    - E75.242 …… type C
    - E75.243 …… type D
    - E75.244 …… type A/B
    - E75.248 Other Niemann-Pick disease
    - E75.249 …… unspecified
  - E75.25 Metachromatic leukodystrophy
  - E75.26 Sulfatase deficiency
  - 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

Disorders of sphingolipid metabolism and other lipid storage disorders E75-

Defects in post-translational modification of lysosomal enzymes

Defects in glycoprotein degradation

Refsum's disease