Hemoglobinopathy, hereditary, NOS: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =Other Hemoglobinopathies| CurrentStatus = | | OldDxArticle =Other Hemoglobinopathies| CurrentStatus = manually added for testing | ||
| InitialEditorAssigned = Elaine Nagy | | InitialEditorAssigned = Elaine Nagy | ||
| MinimumCombinedCodes = | | MinimumCombinedCodes = | ||
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}} | }} | ||
{{ICD10 category|Heme/immunology}}{{ICD10 category|Heredary/congenital}} | |||
== Additional Info == | == Additional Info == | ||
{sc:thalassemia, sickle cell} | {sc:thalassemia, sickle cell} | ||
Revision as of 03:47, 2017 October 16
| ICD10 Diagnosis | |
| Dx: | Hemoglobinopathy, hereditary, NOS |
| ICD10 code: | D58 |
| Pre-ICD10 counterpart: | Other Hemoglobinopathies |
| 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
{sc:thalassemia, sickle cell}
Alternate ICD10s to consider coding instead
(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.) {sc:thalassemia, sickle cell}
Candidate Combined ICD10 codes
(put links to likely candidates coded with this one, eg. a cause for a trauma.)