Hemoglobinopathy, hereditary, NOS: Difference between revisions
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'''Includes:'''<br> | '''Includes:'''<br> | ||
* Hereditary spherocytosis | * Hereditary spherocytosis | ||
* Hb-C | * Hb-C trait | ||
* Hb-D | * Hb-D trait | ||
* Hb-E | * Hb-E trait | ||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
Latest revision as of 12:02, 18 July 2024
| 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: | |
| Data Dependencies(Reports/Indicators/Data Elements): | No results |
| 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.
Includes:
- Hereditary spherocytosis
- Hb-C trait
- Hb-D trait
- Hb-E trait
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
Data Integrity Checks (automatic list)
none found
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