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| General Information | |||
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| Term | Diamond-Blackfan anemia 2 | ID (Ontology) | DOID:0111885 (Human Disease) |
| Definition | A Diamond-Blackfan anemia that has_material_basis_in mutation in a region of chromosome 8p23.3-p22. | ||
| Also Known As | "DBA2" | ||
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| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ pure red-cell aplasia | |__Diamond-Blackfan anemia_____| Diamond-Blackfan anemia 2 |
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| Parents/Children View Depth |
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Relationships
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| Is a |
autosomal dominant disease Diamond-Blackfan anemia |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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MESH:C536130 MIM:606129 |
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