2021 ICD-10-CM Code E75.2

Other sphingolipidosis

Version 2021

Not Valid for Submission

E75.2 is a non-specific and non-billable diagnosis code code, consider using a code with a higher level of specificity for a diagnosis of other sphingolipidosis. The code is not specific and is NOT valid for the year 2021 for the submission of HIPAA-covered transactions. Category or Header define the heading of a category of codes that may be further subdivided by the use of 4th, 5th, 6th or 7th characters.

Short Description:Other sphingolipidosis
Long Description:Other sphingolipidosis

Code Classification

Specific Coding for Other sphingolipidosis

Non-specific codes like E75.2 require more digits to indicate the appropriate level of specificity. Consider using any of the following ICD-10 codes with a higher level of specificity when coding for other sphingolipidosis:

  • BILLABLE CODE - Use E75.21 for Fabry (-Anderson) disease
  • BILLABLE CODE - Use E75.22 for Gaucher disease
  • BILLABLE CODE - Use E75.23 for Krabbe disease
  • NON-BILLABLE CODE - E75.24 for Niemann-Pick disease
  • BILLABLE CODE - Use E75.240 for Niemann-Pick disease type A
  • BILLABLE CODE - Use E75.241 for Niemann-Pick disease type B
  • BILLABLE CODE - Use E75.242 for Niemann-Pick disease type C
  • BILLABLE CODE - Use E75.243 for Niemann-Pick disease type D
  • BILLABLE CODE - Use E75.248 for Other Niemann-Pick disease
  • BILLABLE CODE - Use E75.249 for Niemann-Pick disease, unspecified
  • BILLABLE CODE - Use E75.25 for Metachromatic leukodystrophy
  • BILLABLE CODE - Use E75.26 for Sulfatase deficiency
  • BILLABLE CODE - Use E75.29 for Other sphingolipidosis

Tabular List of Diseases and Injuries

The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code E75.2:

Type 1 Excludes

Type 1 Excludes
A type 1 excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

Clinical Information

Information for Patients

Genetic Brain Disorders

Also called: Inborn genetic brain disorders

A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. Genetic brain disorders affect the development and function of the brain.

Some genetic brain disorders are due to random gene mutations or mutations caused by environmental exposure, such as cigarette smoke. Other disorders are inherited, which means that a mutated gene or group of genes is passed down through a family. They can also be due to a combination of both genetic changes and other outside factors.

Some examples of genetic brain disorders include

Many people with genetic brain disorders fail to produce enough of certain proteins that influence brain development and function. These brain disorders can cause serious problems that affect the nervous system. Some have treatments to control symptoms. Some are life-threatening.

[Learn More in MedlinePlus]

Code History

  • FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016 (First year ICD-10-CM implemented into the HIPAA code set)