| Metadata | |
|---|---|
| ID | DOID:0111086 |
| Name | Fanconi anemia complementation group G |
| 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 |
| Xrefs | |
| Synonyms |
FANCG [EXACT] |
| Parent Relationships |
is_a Fanconi anemia is_a monogenic disease |
| Subclass Logical Relationships |
disease has basis in some gene |