Search Ontology:
Human Disease

Fanconi anemia complementation group F

Term ID
DOID:0111088
Synonyms
  • FANCF
Definition
A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCF gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/10615118
References
Ontology
Human Disease   ( DOID:0111088 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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