Q87.85

MED13L syndrome

Billable / specificPOA exempt

Q87.85 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.

Inclusion terms

Applicable to

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

Includes (from Q87)

  • Note: Codes from this chapter are not for use on maternal records

Excludes1

Not coded here — never report together with this code.

Excludes2

Not included here — may be reported together when both conditions exist.

  • inborn errors of metabolism (E70-E88) (from Q87)

Use additional code

Add a code to identify the following, if applicable.

  • code(s) to identify all associated manifestations (from Q87)

Code also

An additional code may be needed.

  • , 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)

Also known as

  • Asadollahi-Rauch syndrome
  • Mediator complex subunit 13L syndrome
  • MED13Lsyndrome
  • Mediator complex subunit 13Lsyndrome
  • Syndrome, MED13L
  • Syndrome, mediator complex subunit 13L

Parent code

  • Q87.8Other specified congenital malformation syndromes, not elsewhere classifiedHeader

Related codes

  • Q87.81Alport syndromeBillable
  • Q87.82Arterial tortuosity syndromeBillable
  • Q87.83Bardet-Biedl syndromeBillable
  • Q87.84Laurence-Moon syndromeBillable
  • Q87.86Kleefstra syndromeBillable
  • Q87.87Hao-Fountain SyndromeBillable
  • Q87.88CTNNB1 syndromeBillable
  • Q87.89Other specified congenital malformation syndromes, not elsewhere classifiedBillable

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