Multi-minicore Disease (MmD) is a hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy. [ Orphanet:598 ]

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0270962 (Orphanet:598)
  • Orphanet:598 (MONDO:equivalentTo)
  • SCTID:55133004 (MONDO:equivalentTo)
  • GARD:0009130 (shared-umls-xref)
  • ICD10:G71.2 (Orphanet:598)
Subsets

ordo_disease

definition

Multi-minicore Disease (MmD) is a hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy.

exactMatch

http://identifiers.org/snomedct/55133004

http://www.orpha.net/ORDO/Orphanet_598

http://linkedlifedata.com/resource/umls/id/C0270962

has exact synonym

multiminicore disease

MmD

multicore disease

multicore myopathy

id

MONDO:0018948