JSON

[X] familial cardiomyopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0005217

An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

Synonyms: hereditary cardiomyopathy

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:538845 (MONDO:equivalentTo)
  • EFO:0002945 (MONDO:equivalentTo)
  • SCTID:35728003 (MONDO:equivalentTo)
  • icd11.foundation:1018022925 (MONDO:equivalentTo)
  • UMLS:C0264789 (MONDO:equivalentTo)
  • ICD9:425.4 (MONDO:relatedTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_cardiovascular_disorder, mondo_top_grouping_musculoskeletal_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, matrix_txgnn_grouping_member, harrisons_view_cardiovascular_disorder, rare, harrisons_view_member, mondo_top_grouping_cardiovascular_disorder, harrisons_view_musculoskeletal_system_disorder, harrisons_view_hereditary_disease

exactMatch

http://www.ebi.ac.uk/efo/EFO_0002945

http://linkedlifedata.com/resource/umls/id/C0264789

http://identifiers.org/medgen/538845

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1018022925

http://identifiers.org/snomedct/35728003

id

MONDO:0005217