Fanconi anaemia (Q62936): Difference between revisions
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A anemia de Fanconi (AF) é uma doença hereditária de reparo do DNA caracterizada por pancitopenia progressiva com falência da medula óssea, malformações congênitas variáveis e predisposição para desenvolver tumores hematológicos ou sólidos. | |||
| description / en | description / en | ||
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. | |||
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 |
||
| 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. |
