Myofibrillar myopathy   699269005

SNOMED CT code


SNOMED code699269005
nameMyofibrillar myopathy
statusactive
date introduced2014-01-31
fully specified name(s)Myofibrillar myopathy (disorder)
synonymsMyofibrillar myopathy
attributes - group1
Finding siteSkeletal muscle structure   127954009
parentsDisorder of skeletal muscle   75047002
children
  • Alpha-B crystallin-related late-onset myopathy   783770002
  • Autosomal dominant distal axonal motor neuropathy, myofibrillar myopathy syndrome   1179294000
  • Congenital generalized hypercontractile muscle stiffness syndrome   1174000008
  • Desmin-related myofibrillar myopathy   770627003
  • Distal myotilinopathy   765196004
  • Fatal infantile hypertonic myofibrillar myopathy   782883004
  • Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome   1172591008
  • Late-onset distal myopathy Markesbery Griggs type   770558006
  • Muscle filaminopathy   764992006
  • Muscular dystrophy Selcen type   723407009
  • Spheroid body myopathy   765092004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Muscle finding   106030000
      Disorder of muscle   129565002
        Disorder of skeletal muscle   75047002
          Myofibrillar myopathy   699269005

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.