Q85.1
BillableTuberous sclerosis
Q85.1 is the ICD-10-CM code for Tuberous sclerosis. It is a billable, specific code valid for reimbursement.
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities
What this means — in plain language
MedlinePlus · NIHTuberous sclerosis is a rare genetic disease that causes benign tumors to grow in the brain and other organs. Symptoms vary, depending on where the tumors grow. They could include: Skin problems, such as light patches and thickened skin Seizures Behavior problems Intellectual disabilities Kidney problems Some people have signs of tuberous sclerosis at birth. In others it can take time for the symptoms to develop.…
Read more about Tuberous Sclerosis at MedlinePlus ↗Source: U.S. National Library of Medicine (MedlinePlus). Informational only — not medical advice.
Includes
- •Bourneville's disease
- •Epiloia
Medications indicated for this condition
FDA labeling- Interferon Gamma-1bInterferon gamma [EPC]›
- MirdametinibKinase Inhibitor [EPC]›
- SelumetinibKinase Inhibitor [EPC]›
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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