E75.249
BillableNiemann-Pick disease, unspecified
E75.249 is the ICD-10-CM code for Niemann-Pick disease, unspecified. It is a billable, specific code valid for reimbursement.
E00-E89 Endocrine, nutritional and metabolic diseases
What this means — in plain language
MedlinePlus · NIHA 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 (ASMD) NOS
Medications indicated for this condition
FDA labeling- Droxidopa›
- MiglustatGlucosylceramide Synthase Inhibitor [EPC]›
- Arimoclomol›
- EliglustatGlucosylceramide Synthase Inhibitor [EPC]›
- Fosdenopterin›
- LevacetylleucineP-Glycoprotein Inhibitors [MoA]›
- Velmanase Alfa›
Drugs whose FDA labeling lists this condition's category among its indications. Informational only — not a treatment recommendation or medical advice.
Conditions mapped to this code
MedlinePlus · NIHPlain-language health-topic references grounded in MedlinePlus (NIH/NLM).
Frequently asked questions
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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