This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:309279 (MONDO:equivalentTo)
  • UMLS:C5681075 (MONDO:equivalentTo)
  • GARD:10670 (MONDO:GARD)
  • icd11.foundation:979972142 (Orphanet:309279)
  • MEDGEN:1842769 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, disease_grouping, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, 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, ordo_group_of_disorders, harrisons_view_metabolic_disease

comment

See https://github.com/monarch-initiative/monarch-disease-ontology/issues/227

exactMatch

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/979972142

http://www.orpha.net/ORDO/Orphanet_309279

http://linkedlifedata.com/resource/umls/id/C5681075

http://identifiers.org/medgen/1842769

id

MONDO:0017731

seeAlso

https://rarediseases.info.nih.gov/diseases/10670/glycoproteinosis

Term relations