Q87.40
BillableMarfan syndrome, unspecified
Marfan syndrome, unspecified
Status
Billable / Specific
Parent Code
Q87.4Coding Notes
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
Related Codes(3)
Also Known As / Clinical Terms(62)
SNOMED CT
- Marfan syndrome19346006
- Marfan's disease19346006
- Marfan's syndrome19346006
- Congenital anomaly of subcutaneous tissue56759000
- Marfan syndrome affecting skin234035006
- Marfan's syndrome affecting skin234035006
- Marfanoid facies248206001
- Marfanoid physique248298009
- Congenital nephritis276585000
- Plexiform neurofibroma403818001
- Lujan-Fryns syndrome422437002
- X-linked intellectual disability with marfanoid habitus422437002
- X-linked mental retardation with marfanoid habitus syndrome422437002
- Congenital inguinal hernia429200006
- Blindness, scoliosis, arachnodactyly syndrome717920004
- Marfanoid habitus with autosomal recessive intellectual disability syndrome733062000
- Marfanoid habitus, intellectual disability autosomal recessive733062000
- Microcephalus, glomerulonephritis, marfanoid habitus syndrome733472005
- Neonatal Marfan syndrome763839005
- Painful orbital and systemic neurofibroma, marfanoid habitus syndrome773642001
- Progeroid and marfanoid aspect, lipodystrophy syndrome773644000
- Marfanoid habitus, inguinal hernia, advanced bone age syndrome782780007
- Marfan syndrome type 11003407000
UMLS
- MARFAN SYNDROMEC0024796
- MFSC0024796
- Marfan SyndromeC0024796
- Marfan syndromeC0024796
- Marfan syndrome, unspecifiedC0024796
- Marfan's SyndromeC0024796
- Marfan's diseaseC0024796
- Marfan's syndromeC0024796
- Marfan's syndrome (disorder)C0024796
- Marfans SyndromeC0024796
- marfan syndromeC0024796
- marfan's diseaseC0024796
- marfan's syndromeC0024796
- marfans syndromeC0024796
Clinical Terms
- Marfanoid habitus, inguinal hernia, advanced bone age syndrome
- Marfan's syndrome affecting skin
- Neonatal Marfan syndrome
- Marfanoid physique
- Plexiform neurofibroma
- Marfan syndrome type 1
- Painful orbital and systemic neurofibroma, marfanoid habitus syndrome
- Congenital inguinal hernia
- Marfan's Syndrome
- X-linked mental retardation with marfanoid habitus syndrome
- Marfanoid facies
- Lujan-Fryns syndrome
- Marfan's disease
- X-linked intellectual disability with marfanoid habitus
- Marfanoid habitus, intellectual disability autosomal recessive
- Marfanoid habitus with autosomal recessive intellectual disability syndrome
- Congenital anomaly of subcutaneous tissue
- Marfan syndrome affecting skin
- Marfans Syndrome
- Microcephalus, glomerulonephritis, marfanoid habitus syndrome
- MFS
- Congenital nephritis
- Marfan's syndrome (disorder)
- Blindness, scoliosis, arachnodactyly syndrome
- Progeroid and marfanoid aspect, lipodystrophy syndrome
Frequently Asked Questions
What is the ICD-10 code for marfan syndrome, unspecified?
The ICD-10-CM code for marfan syndrome, unspecified is Q87.40. The full clinical description is "Marfan syndrome, unspecified". Q87.40 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q87.40 mean?
ICD-10-CM code Q87.40 represents “Marfan syndrome, unspecified”. 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 Q87.40 a billable code?
Yes, Q87.40 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q87.40 in?
Q87.40 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
Are additional codes required with Q87.40?
Yes, when using Q87.40, also report: code(s) to identify all associated manifestations.
What SNOMED CT codes does Q87.40 map to?
Q87.40 maps to 17 SNOMED CT concepts: 717920004, 56759000, 429200006, 276585000, 422437002, and 12 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q87.40?
Q87.40 is linked to 1 UMLS Concept Unique Identifier: C0024796. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q87.40 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like marfan syndrome, unspecified 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 Q87.40?
There is no direct ICD-11 mapping available for Q87.40 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.