Haemoglobin C/beta thalassaemia compound heterozygosity (Q39521): Difference between revisions
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Latest revision as of 04:58, 13 August 2026
Haemoglobin C/beta thalassaemia is a condition resulting from coinheritance of haemoglobin C and beta thalassaemia, both beta globin genes being mutated.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A51.B |
||
| English | Haemoglobin C/beta thalassaemia compound heterozygosity |
Haemoglobin C/beta thalassaemia is a condition resulting from coinheritance of haemoglobin C and beta thalassaemia, both beta globin genes being mutated. |
Statements
CID11:3A51.B
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dki-india-3A51.B
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Concluído
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13 August 2026
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