Sickle cell disorder or manifestation, NOS: Difference between revisions
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{{ICD10 category|Heme/immunology}}{{ICD10 category|Hereditary/congenital}} | {{ICD10 category|Heme/immunology}}{{ICD10 category|Hereditary/congenital}}{{ICD10 category|Anemia}} | ||
== Additional Info == | == Additional Info == | ||
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*[[Sickle cell crisis]] | *[[Sickle cell crisis]] | ||
*[[Sickle cell anemia, chronic, without crisis]] | *[[Sickle cell anemia, chronic, without crisis]] | ||
* Other Anemias ([[:Category:Anemia]]) | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == |
Revision as of 23:20, 2017 November 11
ICD10 Diagnosis | |
Dx: | Sickle cell disorder or manifestation, NOS |
ICD10 code: | D57.8 |
Pre-ICD10 counterpart: | Sickle Cell Anemia |
Charlson/ALERT Scale: | none |
APACHE Como Component: | none |
APACHE Acute Component: | none |
Start Date: | |
Stop Date: | |
External ICD10 Documentation |
This diagnosis is a part of ICD10 collection.
Additional Info
- Sickle cell anemia is caused by an abnormal type of hemoglobin called hemoglobin S. Hemoglobin is a protein inside red blood cells that carries oxygen. Hemoglobin S changes the red blood cells. The red blood cells become fragile and shaped like crescents or sickles.
Alternate ICD10s to consider coding instead or in addition
- Other Anemias (Category:Anemia)
Candidate Combined ICD10 codes
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