JSON

inborn mitochondrial myopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0009637

Myopathy caused by mitochondrial abnormalities. [ NCIT:C101328 ]

Synonyms: mitochondrial myopathy mitochondrial cytopathy

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:699 (MONDO:equivalentTo)
  • MEDGEN:56484 (MONDO:equivalentTo)
  • NCIT:C101328 (MONDO:equivalentTo)
  • MedDRA:10027710 (Orphanet:206966/e)
  • Orphanet:206966 (MONDO:equivalentTo)
  • GARD:20371 (MONDO:GARD)
  • icd11.foundation:601991549 (https://orcid.org/0000-0002-4142-7153)
  • UMLS:C0162670 (MONDO:equivalentTo)
  • MESH:D017240 (Orphanet:206966/e)
Subsets

gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10027710

exactMatch

http://purl.obolibrary.org/obo/NCIT_C101328

http://identifiers.org/medgen/56484

http://linkedlifedata.com/resource/umls/id/C0162670

http://identifiers.org/mesh/D017240

http://purl.obolibrary.org/obo/DOID_699

http://www.orpha.net/ORDO/Orphanet_206966

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0016117

id

MONDO:0009637