• GARD:1109 (MONDO:GARD)

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, obsoletion_candidate, matrix_llm__tag_existing_treatment_other, matrix_included, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_metabolic_disease, matrix_txgnn_grouping_metabolic_disease, matrix_txgnn_grouping_member, rare, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, harrisons_view_metabolic_disease, mondo_top_grouping_syndromic_disease

• [X] syndromic disease
• [X] inborn errors of metabolism
• disease has feature some [X] hypogonadism
• disease has feature some [X] cardiomyopathy