Hemoglobinopathy, hereditary, NOS: Difference between revisions
Ttenbergen (talk | contribs) m Text replacement - "== Related CCI Codes ==" to "== Related CCI Codes ==" |
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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.<br><br> | |||
'''Includes:'''<br> | |||
* Hereditary spherocytosis | |||
* Hb-C trait | |||
* Hb-D trait | |||
* Hb-E trait | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
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== Related CCI Codes == | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
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