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| Term | multiple types of congenital heart defects 6 | ID (Ontology) | DOID:0060772 (Human Disease) |
| Definition | A congenital heart disease that is characterized by a congenital cardiac malformation characterized by atrioventricular concordance and ventriculoarterial discordance and that has_material_basis_in heterozygous mutation in the GDF1 gene on chromosome 19p13. | ||
| Also Known As | "dextro-looped transposition of the great arteries 3" ; "DTGA3" | ||
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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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autosomal genetic disease |__autosomal dominant disease__ physical disorder | |__congenital heart disease____| heart disease | |__congenital heart disease____| multiple types of congenital heart defects 6 |
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| Is a |
autosomal dominant disease congenital heart disease |
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ICD10CM:Q20.3 MIM:613854 |
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