Marfan syndrome: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
Ttenbergen (talk | contribs) m adding {{Data Integrity Check List}} |
||
| (7 intermediate revisions by 4 users not shown) | |||
| Line 1: | Line 1: | ||
{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle = | | OldDxArticle = Marfan Syndrome | ||
| CurrentStatus = | | CurrentStatus = reconciled | ||
| InitialEditorAssigned = | | InitialEditorAssigned = not assigned | ||
}} | }} | ||
{{ICD10 dx | {{ICD10 dx | ||
| MinimumCombinedCodes = | | MinimumCombinedCodes = | ||
| ICD10 Code=Q87.4 | | ICD10 Code=Q87.4 | ||
| BugRequired= | | BugRequired= | ||
}} | }} | ||
{{ICD10 category|Cardiovascular}}{{ICD10 category|Hereditary/congenital | {{ICD10 category|Cardiovascular}}{{ICD10 category|Hereditary/congenital}} | ||
== Additional Info == | == Additional Info == | ||
[https://en.wikipedia.org/wiki/Marfan_syndrome Marfan syndrome on wikipedia] | |||
*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 == | == 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 | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} | ||
Latest revision as of 01:19, 18 November 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.
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
Data Integrity Checks (automatic list)
none found
Related Articles
| Related articles: |
Show all ICD10 Subcategories
|
ICD10 Categories: |