• MEDGEN:814824 (MONDO:equivalentTo)
• OMIM:614332 (MONDO:equivalentTo)
• UMLS:C3808494 (MONDO:equivalentTo)

matrix_llm__is_cancer_other, gard_rare, mondo_top_grouping_member, matrix_llm__txgnn_other, harrisons_view_psychiatric_disorder, nord_rare, matrix_included, matrix_txgnn_grouping_member, rare, matrix_txgnn_grouping_psychiatric_disorder, harrisons_view_nervous_system_disorder, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, harrisons_view_chromosomal_disorder, mondo_top_grouping_chromosomal_disorder, matrix_llm__tag_existing_treatment_other, mondo_top_grouping_psychiatric_disorder, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, harrisons_view_hereditary_disease

• [X] syndrome caused by partial chromosomal deletion and disease arises from alteration in structure some 2p16.3 (Human)

• [X] hereditary neurological disease
• [X] partial deletion of the short arm of chromosome 2
• schizophrenia
• disease arises from alteration in structure some 2p16.3 (Human)
• has material basis in germline mutation in some NRXN1