• UMLS:C2751682 (MONDO:equivalentTo)
• MEDGEN:416607 (MONDO:equivalentTo)
• OMIM:613013 (MONDO:equivalentTo)

matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__is_glucose_dysfunction_other, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, susceptibility_mondo, inferred_rare, matrix_included, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, susceptibility_match, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, harrisons_view_cancer_or_benign_tumor, rare, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, mondo_top_grouping_syndromic_disease

• inherited disease susceptibility and has material basis in germline mutation in some PHOX2B and predisposes towards some neuroblastoma

• [X] hereditary neoplastic syndrome
• predisposes towards some neuroblastoma
• has material basis in germline mutation in some PHOX2B