Fanconi anemia complementation group D2
Information
- Disease name
- Fanconi anemia complementation group D2
- Disease ID
- DOID:0111083
- Description
- "A Fanconi anemia that has_material_basis_in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25." [url:https\://www.ncbi.nlm.nih.gov/pubmed/11239453, url:https\://www.ncbi.nlm.nih.gov/pubmed/17436244]
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:227646
- Exact Synonym (Disease Ontology)
- FA4
- Exact Synonym (Disease Ontology)
- FAD2
- Exact Synonym (Disease Ontology)
- FANCD2
- Exact Synonym (Disease Ontology)
- Fanconi pancytopenia type 4