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Q87.85 MED13L syndrome

BackQ87Other specified congenital malformation syndromes affecting multiple systems7 →Q87.0Congenital malformation syndromes predominantly affecting facial appearanceQ87.1Congenital malformation syndromes predominantly associated with short stature2 →Q87.11Prader-Willi syndromeQ87.19Other congenital malformation syndromes predominantly associated with short statureQ87.2Congenital malformation syndromes predominantly involving limbsQ87.3Congenital malformation syndromes involving early overgrowthQ87.4Marfan syndrome4 →Q87.40Marfan syndrome, unspecifiedQ87.41Marfan syndrome with cardiovascular manifestations2 →Q87.410Marfan syndrome with aortic dilationQ87.418Marfan syndrome with other cardiovascular manifestationsQ87.42Marfan syndrome with ocular manifestationsQ87.43Marfan syndrome with skeletal manifestationQ87.5Other congenital malformation syndromes with other skeletal changesQ87.8Other specified congenital malformation syndromes, not elsewhere classified9 →Q87.81Alport syndromeQ87.82Arterial tortuosity syndromeQ87.83Bardet-Biedl syndromeQ87.84Laurence-Moon syndromeQ87.85MED13L syndromeQ87.86Kleefstra syndromeQ87.87Hao-Fountain SyndromeQ87.88CTNNB1 syndromeQ87.89Other specified congenital malformation syndromes, not elsewhere classified
CategoryCODABLE
Q87.85
MED13L syndrome
EXAMPLES
Asadollahi-Rauch syndrome
Mediator complex subunit 13L syndrome
CODING RULE
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)
Chapter
XVII · Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders
Section
Q80-Q89
Valid from
Source

CMS ICD-10-CM Tabular List, edition FY2026.

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