Search Ontology:
Human Disease

Fanconi anemia complementation group B

Term ID
DOID:0111098
Synonyms
  • FACB
  • FANCB
  • Fanconi pancytopenia type 2
Definition
A Fanconi anemia that has_material_basis_in mutation in the FANCB gene on chromosome Xp22. https://www.ncbi.nlm.nih.gov/pubmed/15502827
References
Ontology
Human Disease   ( DOID:0111098 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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