JSON

variably protease-sensitive prionopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0018692

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C4303527 (MONDO:equivalentTo)
  • Orphanet:454742 (MONDO:equivalentTo)
  • GARD:21894 (MONDO:GARD)
  • SCTID:721165001 (MONDO:equivalentTo)
  • MEDGEN:929196 (MONDO:equivalentTo)
  • icd11.foundation:172957869 (https://orcid.org/0000-0002-4142-7153)
Subsets

ordo_disorder, gard_rare, harrisons_view_infectious_disease, matrix_llm__medical_specialization_neurology, mondo_top_grouping_member, matrix_llm__medical_specialization_member, matrix_llm__tag_existing_treatment_false, matrix_llm__is_glucose_dysfunction_false, matrix_included, nord_rare, mondo_top_grouping_infectious_disease, matrix_llm__txgnn_prionopathy, matrix_llm__is_glucose_dysfunction_member, matrix_txgnn_grouping_member, matrix_llm__is_pathogen_caused_false, rare, matrix_llm__anatomical_muscle_disorder, orphanet_rare, matrix_llm__tag_qaly_lost_member, harrisons_view_nervous_system_disorder, matrix_llm__anatomical_spinal_disorder, matrix_llm__tag_qaly_lost_high, matrix_llm__tag_qualy_lost_other, matrix_llm__is_cancer_false, matrix_llm__tag_existing_treatment_member, matrix_txgnn_grouping_neurodegenerative_disease, matrix_llm__is_pathogen_caused_member, matrix_llm__txgnn_neurodegenerative_disease, matrix_llm__anatomical_brain_disorder, matrix_txgnn_grouping_infectious_disease, matrix_llm__txgnn_member, harrisons_view_member, mondo_top_grouping_nervous_system_disorder, matrix_llm__is_cancer_member, matrix_llm__medical_specialization_genetics_and_genomics, matrix_llm__anatomical_member

exactMatch

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/172957869

http://identifiers.org/snomedct/721165001

http://www.orpha.net/ORDO/Orphanet_454742

http://linkedlifedata.com/resource/umls/id/C4303527

http://identifiers.org/medgen/929196

id

MONDO:0018692