JSON

inborn mitochondrial myopathy

^ http://purl.obolibrary.org/obo/MONDO_0009637

Myopathy caused by mitochondrial abnormalities. [ NCIT:C101328 ]

Term info

database cross reference
  • NCIT:C101328 (MONDO:equivalentTo)
  • DOID:699 (MONDO:equivalentTo)
  • GARD:0011956 (MONDO:equivalentTo)
  • UMLS:C0162670 (Orphanet:206966/e)
  • MedDRA:10027710 (Orphanet:206966/e)
  • Orphanet:206966 (MONDO:equivalentTo)
  • MESH:D017240 (Orphanet:206966/e)
Subsets

disease_grouping, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10027710

definition

Myopathy caused by mitochondrial abnormalities.

exactMatch

http://purl.obolibrary.org/obo/Orphanet_206966, http://purl.obolibrary.org/obo/NCIT_C101328, http://linkedlifedata.com/resource/umls/id/C0162670, http://identifiers.org/mesh/D017240, http://purl.obolibrary.org/obo/DOID_699

excluded subClassOf

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

has exact synonym

mitochondrial myopathy, mitochondrial cytopathy

id

MONDO:0009637