Hemoglobinopathy, hereditary, NOS
Jump to navigation
Jump to search
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.
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
Related Articles
Show all ICD10 Subcategories