Q87.85

MED13L syndrome

Billable code

This code does not map to a risk-adjusting HCC in the loaded models.

Coding notes

Excludes 1 never coded together · Excludes 2 may co-exist

This code · Q87.85

Code also

, 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)

Synonyms

Asadollahi-Rauch syndrome Mediator complex subunit 13L syndrome

Inherited from Q87.8Oth congenital malformation syndromes, NEC

Excludes 1

Zellweger syndrome (E71.510)

Inherited from Q87Oth congenital malform syndromes affecting multiple systems

Use additional

code(s) to identify all associated manifestations

Inherited from chapter 17Congenital malformations, deformations and chromosomal abnormalities

Excludes 2

inborn errors of metabolism (E70-E88)

Official Guidelines for Q87.85

FY 2026 ›

I.C.17Chapter-specific guidanceChapter 17: Congenital malformations, deformations, and chromosomal abnormalities (Q00-QA1)

Sections that reference Q87.85

IV.QEncounters for routine health screeningsOutpatient services
… Congenital conditions and anomalies Assign “Y” for congenital conditions and anomalies except for categories Q00- Q99, Congenital anomalies, which are on the exempt list. …

Sections whose FY 2026 text names Q87.85, its Q87 category, or a range containing it — the chapter guidance above is the authoritative source.

Find Q87.85 in the alphabetic index

5 index paths lead to this code