Search Ontology:
Human Disease

Fanconi anemia complementation group G

Term ID
DOID:0111086
Synonyms
  • FANCG
Definition
A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the XRCC9 gene on chromosome 9p13. https://www.ncbi.nlm.nih.gov/pubmed/9806548
References
Ontology
Human Disease   ( DOID:0111086 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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