OBO ID: DOID:0111083 |
Term Name: | Fanconi anemia complementation group D2 | Search Ontology: | |
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Synonyms: |
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Definition: | A Fanconi anemia that has_material_basis_in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25. (2) | ||
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Ontology: | Human Disease ( DOID:0111083 ) |
OTHER Fanconi anemia complementation group D2 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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