Fanconi anemia complementation group N
Information
- Disease name
- Fanconi anemia complementation group N
- Disease ID
- DOID:0111094
- Description
- "A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the PALB2 gene on chromosome 16p12." [url:https\://www.ncbi.nlm.nih.gov/pubmed/17200671, url:https\://www.ncbi.nlm.nih.gov/pubmed/17200672]
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:610832
- Exact Synonym (Disease Ontology)
- FANCN