OBO ID: DOID:0111094
Term Name: Fanconi anemia complementation group N Search Ontology:
Synonyms:
  • FANCN
Definition: A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12. (2)
References:
Ontology: Human Disease   (DOID:0111094)
OTHER Fanconi anemia complementation group N PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PALB2 Fanconi anemia, complementation group N 610832
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None