Hemoglobinopathy, hereditary, NOS: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =Other Hemoglobinopathies | | OldDxArticle =Other Hemoglobinopathies | ||
| CurrentStatus = | | CurrentStatus = reconciled | ||
| InitialEditorAssigned = Elaine Nagy | | InitialEditorAssigned = Elaine Nagy | ||
}} | }} | ||
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== Additional Info == | == Additional Info == | ||
The hemoglobinopathies encompass all genetic diseases of hemoglobin. They fall into two main groups: thalassemia syndromes and structural hemoglobin variants (abnormal hemoglobins). α- and β-thalassemia are the main types of thalassemia; the main structural hemoglobin variants are HbS, HbE and HbC. | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
*[[Thalassemia disorder or trait]] | *[[Thalassemia disorder or trait]] |
Revision as of 11:28, 2018 March 29
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
The hemoglobinopathies encompass all genetic diseases of hemoglobin. They fall into two main groups: thalassemia syndromes and structural hemoglobin variants (abnormal hemoglobins). α- and β-thalassemia are the main types of thalassemia; the main structural hemoglobin variants are HbS, HbE and HbC.
Alternate ICD10s to consider coding instead or in addition
- Thalassemia disorder or trait
- Sickle cell anemia, chronic, without crisis
- Sickle cell crisis
- Sickle cell disorder or manifestation, NOS
- Sickle cell trait
- Other Anemias (Category:Anemia)
Candidate Combined ICD10 codes
Related CCI Codes
Related Articles
Show all ICD10 Subcategories