Fanconi anaemia (Q62936): Difference between revisions
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CID11:ID_1500851497 | |||||||||||||||
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dki-india-ID_1500851497 | |||||||||||||||
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13 August 2026
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Latest revision as of 10:25, 14 August 2026
Fanconi anaemia (FA) is a hereditary DNA repair disorder characterised by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop haematological or solid tumours.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1500851497 |
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| English | Fanconi anaemia |
Fanconi anaemia (FA) is a hereditary DNA repair disorder characterised by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop haematological or solid tumours. |
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CID11:ID_1500851497
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dki-india-ID_1500851497
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Concluído
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13 August 2026
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