[X] disorder of metabolite absorption and transport
Go to external page http://purl.obolibrary.org/obo/MONDO_0017757
Term information
- MEDGEN:1842202 (MONDO:equivalentTo)
- Orphanet:309824 (MONDO:equivalentTo)
- GARD:21349 (MONDO:GARD)
- UMLS:C5681033 (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, disease_grouping, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_metabolic_disease, matrix_txgnn_grouping_metabolic_disease, matrix_txgnn_grouping_member, rare, harrisons_view_member, harrisons_view_hereditary_disease, harrisons_view_metabolic_disease, ordo_group_of_disorders
http://identifiers.org/medgen/1842202
http://www.orpha.net/ORDO/Orphanet_309824
http://linkedlifedata.com/resource/umls/id/C5681033