familial isolated dilated cardiomyopathy
Go to external page http://purl.obolibrary.org/obo/MONDO_0700335
A rare familial cardiomyopathy characterized by the dilation of left ventricle and progressively impairing of systolic ventricular function, in the absence of abnormal loading conditions or coronary artery disease sufficient to cause global systolic impairment. The disease may cause heart failure or arrhythmia. The disease is isolated when no additional atypical cardiac or extracardiac manifestations are present. [ Orphanet:154 ]
Synonyms: familial isolated dilated cardiomyopathy familial or idiopathic dilated cardiomyopathy
Term information
- Orphanet:154 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_cardiovascular_disorder, mondo_top_grouping_musculoskeletal_system_disorder, inferred_rare, matrix_included, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, harrisons_view_cardiovascular_disorder, rare, harrisons_view_member, mondo_top_grouping_cardiovascular_disorder, harrisons_view_musculoskeletal_system_disorder, harrisons_view_hereditary_disease
https://github.com/monarch-initiative/mondo/issues/6877
https://github.com/monarch-initiative/mondo/issues/6740
https://github.com/monarch-initiative/mondo/issues/6751
https://github.com/monarch-initiative/mondo/issues/5114
https://github.com/monarch-initiative/mondo/issues/7693