Marfan syndrome: Difference between revisions
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Revision as of 15:47, 31 October 2018
| ICD10 Diagnosis | |
| Dx: | Marfan syndrome |
| ICD10 code: | Q87.4 |
| Pre-ICD10 counterpart: | Marfan Syndrome |
| 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.
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.
Alternate ICD10s to consider coding instead or in addition
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 Articles
| Related articles: |
Show all ICD10 Subcategories