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| Term | right atrial isomerism | ID (Ontology) | DOID:0060856 (Human Disease) |
| Definition | A visceral heterotaxy that is characterized by complete atrioventricular septal defect with a common atrium and univentricular AV connection, total anomalous pulmonary drainage, and transposition or malposition of the great arteries and that has_material_basis_in homozygous mutation in the GDF1 gene on chromosome 19p12. | ||
| Also Known As | "asplenia with cardiovascular anomalies" ; "Ivemark syndrome" | ||
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autosomal genetic disease |__autosomal recessive disease__ physical disorder | |__visceral heterotaxy__________| right atrial isomerism |
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| Is a |
visceral heterotaxy autosomal recessive disease |
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ICD10CM:Q20.6 MIM:208530 ORDO:97548 |
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