OBO ID: DOID:0060772 |
Term Name: | multiple types of congenital heart defects 6 | Search Ontology: | |
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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. https://www.ncbi.nlm.nih.gov/pubmed/17924340 | ||
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Ontology: | Human Disease ( DOID:0060772 ) |
OTHER multiple types of congenital heart defects 6 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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GDF1 | Congenital heart defects, multiple types, 6 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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