Marfan syndrome: Difference between revisions

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== Additional Info ==
== Additional Info ==
**Marfan syndrome (or Marfan's syndrome) is a genetic disorder of the connective tissue.
*People with Marfan's are typically tall, with long limbs and long thin fingers.


*The most serious complication is defects of the heart valves and aorta. It may also affect the lungs, eyes, the dural sac surrounding the spinal cord, skeleton and the hard palate.
[https://en.wikipedia.org/wiki/Marfan_syndrome Marfan syndrome]
== Alternate ICD10s to consider coding instead or in addition ==
== Alternate ICD10s to consider coding instead or in addition ==


== Candidate [[Combined ICD10 codes]] ==
== Candidate [[Combined ICD10 codes]] ==
*[[Mitral valve prolapse]]
*[[Aortic aneurysm, NOS with rupture]]
*[[Aortic aneurysm, NOS without mention of rupture]]
*[[Aortic aneurysm, thoracic without mention of rupture]]
*[[Aortic aneurysm, thoracic with rupture]]


== Related CCI Codes ==
== Related CCI Codes ==

Revision as of 11:05, 17 May 2018

ICD10 Diagnosis
Dx: Marfan syndrome
ICD10 code: Q87.4
Pre-ICD10 counterpart: none assigned
Charlson/ALERT Scale: none
APACHE Como Component: none
APACHE Acute Component: none
Start Date:
Stop Date:
Data Dependencies(Reports/Indicators/Data Elements): No results
External ICD10 Documentation

This diagnosis is a part of ICD10 collection.

  • SMW
    • 2019-01-01
    • 2999-12-31
    • Q87.4
  • Cargo


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Additional Info

    • Marfan syndrome (or Marfan's syndrome) is a genetic disorder of the connective tissue.
  • People with Marfan's are typically tall, with long limbs and long thin fingers.
  • The most serious complication is defects of the heart valves and aorta. It may also affect the lungs, eyes, the dural sac surrounding the spinal cord, skeleton and the hard palate.


Marfan syndrome

Alternate ICD10s to consider coding instead or in addition


Related articles:


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