3A50 Thalassaemias
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
A disease caused by genetically inherited autosomal recessive mutations leading to abnormal production of haemoglobin. This disease is characterised by destruction of red blood cells leading to anaemia and abnormal production of haemoglobin. This disease may present with pallor, jaundice, iron overload, fatigue, or shortness of breath. Confirmation is by identification of mutations through genetic testing.
sections/codes in this section (3A50-3A50)
- Alpha thalassaemia (3A50.0)
- Alpha thalassaemia related syndromes (3A50.1)
- Beta thalassaemia (3A50.2)
- Delta, delta-beta or gamma-delta-beta thalassaemia (3A50.3)
- Hereditary persistence of fetal haemoglobin (3A50.4)
- Other specified thalassaemias (3A50.Y)
- Thalassaemias, unspecified (3A50.Z)
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
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