JSON

disorder of mineral absorption and transport

Go to external page http://purl.obolibrary.org/obo/MONDO_0017761

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1842552 (MONDO:equivalentTo)
  • UMLS:C5681035 (MONDO:equivalentTo)
  • ICD10CM:E83.3 (Orphanet:309836/specific)
  • GARD:21353 (MONDO:GARD)
  • icd11.foundation:1833416892 (https://orcid.org/0000-0002-4142-7153)
  • Orphanet:309836 (MONDO:equivalentTo)
  • ICD10CM:E83.1 (Orphanet:309836/specific)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, 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_included, 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

exactMatch

http://www.orpha.net/ORDO/Orphanet_309836

http://identifiers.org/medgen/1842552

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1833416892

http://linkedlifedata.com/resource/umls/id/C5681035

id

MONDO:0017761