A congenital disorder characterized by the presence of an abnormal communication between the atria or the ventricles of the heart due to defects in the cardiac septum. [ NCIT:P378 ]
Synonyms: holes in the heart congenital septal defect congenital septal defect of heart Cardiac septal defects septal defect
Term information
- ICD9:745.8 (MONDO:relatedTo)
- MESH:D006343 (MONDO:equivalentTo)
- ICD9:745.9 (MONDO:i2s)
- DOID:1681 (MONDO:equivalentTo)
- UMLS:C0018816 (MONDO:equivalentTo)
- SCTID:253273004 (MONDO:equivalentTo)
- MEDGEN:6752 (MONDO:equivalentTo)
- NCIT:C84482 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_txgnn_grouping_cardiovascular_disorder, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cardiovascular_disorder, matrix_txgnn_grouping_member, harrisons_view_member, mondo_top_grouping_cardiovascular_disorder, mondo_top_grouping_disorder_of_development_or_morphogenesis
http://identifiers.org/snomedct/253273004
http://purl.obolibrary.org/obo/NCIT_C84482
http://linkedlifedata.com/resource/umls/id/C0018816
http://identifiers.org/mesh/D006343
http://purl.obolibrary.org/obo/DOID_1681
http://identifiers.org/medgen/6752