• Orphanet:500180 (OMIM:617672)
• DOID:0070474 (MONDO:equivalentTo)
• MEDGEN:1626007 (MONDO:equivalentTo)
• OMIM:617672 (Orphanet:500180)
• UMLS:C4540086 (MONDO:equivalentTo)
• GARD:13658 (MONDO:GARD)

matrix_llm__is_cancer_other, ordo_disorder, gard_rare, matrix_llm__is_glucose_dysfunction_other, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, nord_rare, matrix_llm__tag_existing_treatment_other, matrix_included, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_hereditary_disease, orphanet_rare, harrisons_view_nervous_system_disorder

• [X] movement disorder
• [X] hereditary neurological disease
• [X] central nervous system malformation
• [X] congenital nervous system disorder
• [X] multiple congenital anomalies/dysmorphic syndrome-intellectual disability
• disease has major feature some [X] central nervous system malformation
• has material basis in germline mutation in some UBTF
• disease arises from feature some [X] neurodegenerative disease