DISEASES

Disease-gene associations mined from literature

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