(Q32146879)
English
Fanconi anemia complementation group L
Fanconi anemia that has material basis in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16
- FANCL
- FANCONI ANEMIA, COMPLEMENTATION GROUP L; FANCL
- Fanconi anemia complementation group type L
- Fanconi Anemia, Complementation Group type 50
- FANCONI ANEMIA, COMPLEMENTATION GROUP L
Statements
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C164677
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Identifiers
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