OBO ID: DOID:0111086
Term Name: Fanconi anemia complementation group G Search Ontology:
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 Fanconi anemia complementation group G PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FANCG Fanconi anemia, complementation group G 614082
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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