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Q87.85

Billable

MED13L syndrome

Q87.85 is the ICD-10-CM code for MED13L syndrome. It is a billable, specific code valid for reimbursement.

Status
Billable
Chapter
Q00-Q99
Parent
Q87.8
Edition
FY2026

Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities

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Includes

  • •Asadollahi-Rauch syndrome
  • •Mediator complex subunit 13L syndrome

Notes

  • •, if applicable, any associated manifestations such as:
  • •autism spectrum disorder (F84.0-)
  • •congenital malformations of cardiac septa (Q21.-)
  • •epilepsy and recurrent seizures (G40.-)
  • •intellectual disability (F70-F79)

Medications indicated for this condition

FDA labeling

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 · NIH
Marfan SyndromePrader-Willi Syndrome

Plain-language health-topic references grounded in MedlinePlus (NIH/NLM).

Frequently asked questions

What is ICD-10 code Q87.85?
Q87.85 is the ICD-10-CM code for "MED13L syndrome". It falls under Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities.
Is Q87.85 a billable code?
Yes — Q87.85 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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