Search Ontology:
Human Disease

Fanconi anemia complementation group L

Term ID
DOID:0111082
Synonyms
  • FANCL
Definition
A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16. (2)
References
Ontology
Human Disease   ( DOID:0111082 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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