Fanconi anemia complementation group G
Information
- Disease name
- Fanconi anemia complementation group G
- Disease ID
- DOID:0111086
- Description
- "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the XRCC9 gene on chromosome 9p13." [url:https\://www.ncbi.nlm.nih.gov/pubmed/9806548]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:13636
- Cross Reference ID (Disease Ontology)
- MIM:614082
- Exact Synonym (Disease Ontology)
- FANCG