Synonyms: cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency cardiomyopathy with myopathy due to COX deficiency Leigh disease with myopathy
Term information
- Orphanet:70474 (MONDO:equivalentObsolete)
- GARD:16685 (MONDO:GARD)
- icd11.foundation:583594497 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__txgnn_other, mondo_top_grouping_member, nord_rare, matrix_included, mondo_top_grouping_metabolic_disease, matrix_txgnn_grouping_member, rare, harrisons_view_mitochondrial_disease, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, mondo_top_grouping_mitochondrial_disease, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_metabolic_disease, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_metabolic_disease