• MEDGEN:1823994 (MONDO:equivalentTo)
• OMIM:620049 (MONDO:equivalentTo)
• UMLS:C5774221 (MONDO:equivalentTo)

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, mondo_top_grouping_urinary_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_included, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_urinary_system_disorder, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, mondo_top_grouping_syndromic_disease

• [X] familial nephrotic syndrome
• has material basis in germline mutation in some LAMA5