3A51.3 Compound heterozygous sickling disorders without crisis

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01


A disease caused by genetic inheritance of two heterozygous recessive alleles of the haemoglobin gene leading to abnormal formation of haemoglobin molecule. This disease is characterised by rigid, sickle shaped red blood cells. Confirmation is by identification of mutations through genetic testing.

inclusions

postcoordination

Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.

Has manifestation  - multiple selections are allowed

synonyms

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