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| Term | visceral heterotaxy 4 | ID (Ontology) | DOID:0051019 (Human Disease) |
| Definition | A visceral heterotaxy that is has_material_basis_in heterozygous mutation in the ACVR2B gene on chromosome 3p22. | ||
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| DO.org | |||
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| 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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physical disorder |__visceral heterotaxy |__visceral heterotaxy 4 1 rec. |
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Relationships
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| Is a | visceral heterotaxy | ||
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External Crossreferences & Linkouts
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| MIM:613751 | |||