Human genes for Fanconi anemia complementation group L
Fanconi anemia complementation group L [DOID:0111082]
A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16.
Synonyms: Fanconi anemia complementation group L, DOID:0111082, Fanconi anemia complementation group Ls, FANCLs