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| Term | atrial heart septal defect 8 | ID (Ontology) | DOID:0110113 (Human Disease) |
| Definition | An atrial heart septal defect that has_material_basis_in heterozygous mutation in the CITED2 gene on chromosome 6q23.3. | ||
| Also Known As | "ASD8" ; "atrial septal defect 8" | ||
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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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autosomal genetic disease |__autosomal dominant disease__ heart septal defect | |__atrial heart septal defect__| atrial heart septal defect 8 |
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| Is a |
autosomal dominant disease atrial heart septal defect |
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ICD10CM:Q21.1 MIM:614433 |
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