Term information
- Orphanet:289635 (MONDO:equivalentTo)
- MEDGEN:1842723 (MONDO:equivalentTo)
- UMLS:C5681008 (MONDO:equivalentTo)
- GARD:21145 (MONDO:GARD)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_excluded, mondo_top_grouping_post_infectious_disorder, otar, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, ordo_group_of_disorders
http://linkedlifedata.com/resource/umls/id/C5681008
http://www.orpha.net/ORDO/Orphanet_289635
http://identifiers.org/medgen/1842723