E75.244

Billable

Niemann-Pick disease type A/B

E75.244 is the ICD-10-CM code for Niemann-Pick disease type A/B. It is a billable, specific code valid for reimbursement.

Status
Billable
Chapter
E00-E89
Parent
E75.24
Edition
FY2026

E00-E89 Endocrine, nutritional and metabolic diseases

What this means — in plain language

MedlinePlus · NIH

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…

Read more about Genetic Brain Disorders at MedlinePlus ↗

Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.

Includes

  • Acid sphingomyelinase deficiency type A/B (ASMD type A/B)
  • Chronic neurovisceral acid sphingomyelinase deficiency

Frequently asked questions

What is ICD-10 code E75.244?
E75.244 is the ICD-10-CM code for "Niemann-Pick disease type A/B". It falls under E00-E89 Endocrine, nutritional and metabolic diseases.
Is E75.244 a billable code?
Yes — E75.244 is a billable, specific ICD-10-CM code valid for reimbursement.

Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.

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