Fanconi anemia complementation group D1
Information
- Disease name
- Fanconi anemia complementation group D1
- Disease ID
- DOID:0111089
- Description
- "A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRCA2 gene on chromosome 13q13." [url:https\://www.ncbi.nlm.nih.gov/pubmed/12065746, url:https\://www.ncbi.nlm.nih.gov/pubmed/14670928]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes | Mutation | Description | Source | Links |
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- Disase is a (Disease Ontology)
- DOID:13636
- Cross Reference ID (Disease Ontology)
- MIM:605724
- Exact Synonym (Disease Ontology)
- FAD1
- Exact Synonym (Disease Ontology)
- FANCD1