Search Ontology:
Human Disease

Fanconi anemia complementation group N

Term ID
DOID:0111094
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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