Q87.85
BillableMED13L syndrome
MED13L syndrome
Status
Billable / Specific
Parent Code
Q87.8Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Asadollahi-Rauch syndrome
- Mediator complex subunit 13L syndrome
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
Use Additional Code
Additional codes that should follow this code
- code(s) to identify all associated manifestations
Code Also
A second code may be required; sequencing depends on circumstances
- , if applicable, any associated manifestations such as:
- •autism spectrum disorderF84.0
- •congenital malformations of cardiac septaQ21
- •epilepsy and recurrent seizuresG40
- •intellectual disabilityF70-F79
Related Codes(6)
Also Known As / Clinical Terms(30)
UMLS
- ASADOLLAHI-RAUCH SYNDROMEC5192431
- ASRASC5192431
- Asadollahi-Rauch syndromeC5192431
- Cardiac anomalies-developmental delay-facial dysmorphism syndromeC5192431
- Developmental delay, facial dysmorphism syndrome due to MED13L deficiencyC5192431
- Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiencyC5192431
- Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder)C5192431
- Developmental delay-facial dysmorphism syndrome due to MED13L deficiencyC5192431
- IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTSC5192431
- Intellectual disability and distinctive facial features with or without cardiac defectsC5192431
- MED13L haploinsufficiency syndromeC5192431
- MED13L syndromeC5192431
- MED13L-related intellectual disabilityC5192431
- MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTSC5192431
- MRFACDC5192431
- Mediator complex subunit 13L syndromeC5192431
Clinical Terms
- ASADOLLAHI-RAUCH SYNDROME
- Cardiac anomalies-developmental delay-facial dysmorphism syndrome
- IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS
- Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency (disorder)
- Developmental delay, facial dysmorphism syndrome due to MED13L deficiency
- MED13L haploinsufficiency syndrome
- Developmental delay, facial dysmorphism syndrome due to mediator complex subunit 13 like deficiency
- Developmental delay-facial dysmorphism syndrome due to MED13L deficiency
- Intellectual disability and distinctive facial features with or without cardiac defects
- MRFACD
- MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS
- ASRAS
- Mediator complex subunit 13L syndrome
- MED13L-related intellectual disability
Frequently Asked Questions
What is the ICD-10 code for med13l syndrome?
The ICD-10-CM code for med13l syndrome is Q87.85. The full clinical description is "MED13L syndrome". Q87.85 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q87.85 mean?
ICD-10-CM code Q87.85 represents “MED13L syndrome”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q87.85 a billable code?
Yes, Q87.85 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q87.85 in?
Q87.85 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q87.85?
Q87.85 has Excludes1 notes indicating codes that cannot be used together with it, including: Zellweger syndrome (E71.510).
Are additional codes required with Q87.85?
Yes, when using Q87.85, also report: code(s) to identify all associated manifestations.
What are the UMLS CUIs for Q87.85?
Q87.85 is linked to 1 UMLS Concept Unique Identifier: C5192431. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q87.85 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like med13l syndrome affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q87.85?
There is no direct ICD-11 mapping available for Q87.85 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.