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General Information
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| Term |
Fanconi anemia complementation group D2 |
ID (Ontology) |
DOID:0111083 (Human Disease) |
| Definition |
A Fanconi anemia that has_material_basis_in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25. |
| Also Known As |
"FA4" ; "FAD2" ; "FANCD2" (for all, see Synonyms field below) |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 4 | | Human Disease Models (FBhh) | DOID | 1 |
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Alleles | Genes | Human Disease Models |
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Fanconi anemia complementation group D2 | 4 | 1 | 1 | for disease ribbon | Fanconi anemia complementation group D2 | -- | 1 | -- | model of | Fanconi anemia complementation group D2 | 4 | 1 | -- |
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Relationships