Term information
- Orphanet:171898 (MONDO:equivalentTo)
- MEDGEN:1842533 (MONDO:equivalentTo)
- GARD:20131 (MONDO:GARD)
- UMLS:C5680515 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, matrix_llm__tag_qualy_lost_other, disease_grouping, mondo_top_grouping_hematologic_disorder, 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, harrisons_view_hematologic_disorder, matrix_txgnn_grouping_member, harrisons_view_cancer_or_benign_tumor, rare, harrisons_view_member, ordo_group_of_disorders
http://linkedlifedata.com/resource/umls/id/C5680515
http://identifiers.org/medgen/1842533
http://www.orpha.net/ORDO/Orphanet_171898
https://github.com/monarch-initiative/mondo/issues/6739
https://github.com/monarch-initiative/mondo/issues/6746