Term Name: Fanconi anemia complementation group N
Synonyms: FANCN
Definition: A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12.
Ontology: Human Disease [DOID:0111094]   (DOID:0111094)

Relationships
is a type of: Fanconi anemia monogenic disease