FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term atrial heart septal defect 7 ID (Ontology) DOID:0110112 (Human Disease)
Definition An atrial heart septal defect that has_material_basis_in heterozygous mutation in the NKX2-5 gene on chromosome 5q35.
Also Known As "ASD with or without atrioventricular conduction defects" ; "atrial septal defect 7, with or without AV conduction defects" ; "atrial septal defect-atrioventricular conduction defects syndrome"
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 Genes
 atrial heart septal defect 7       2
 for disease ribbon | atrial heart septal defect 7       2
 model of | atrial heart septal defect 7       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
heart septal defect             |
 |__atrial heart septal defect__|
                                atrial heart septal defect 7  2 rec.
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Is a autosomal dominant disease
atrial heart septal defect
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Synonyms
  • "ASD with or without atrioventricular conduction defects" EXACT
    "atrial septal defect 7, with or without AV conduction defects" EXACT
    "atrial septal defect-atrioventricular conduction defects syndrome" EXACT
Secondary IDs
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ICD10CM:Q21.1
MIM:108900
ORDO:1479