E75.22
BillableGaucher disease
E75.22 is the ICD-10-CM code for Gaucher disease. It is a billable, specific code valid for reimbursement.
E00-E89 Endocrine, nutritional and metabolic diseases
What this means — in plain language
MedlinePlus · NIHGaucher disease is a rare, inherited disorder. It is a type of lipid metabolism disorder . If you have it, you do not have enough of an enzyme called glucocerebrosidase. This causes too much of a fatty substance to build up in your spleen, liver, lungs, bones and, sometimes, your brain. This prevents these organs from working properly. There are three types: Type 1, the most common form, causes liver and spleen…
Read more about Gaucher Disease at MedlinePlus ↗Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.
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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