SNOMED CT Concept  138875005

Clinical finding  404684003

Muscle finding  106030000

Disorder of muscle  129565002

Disorder of skeletal muscle  75047002

Congenital anomaly of skeletal muscle  89886004

Congenital hereditary muscular dystrophy  111501005

Congenital muscular dystrophy with arthrogryposis multiplex congenita   240061000

SNOMED CT code


SNOMED code240061000
nameCongenital muscular dystrophy with arthrogryposis multiplex congenita
statusactive
date introduced2002-01-31
fully specified name(s)Congenital muscular dystrophy with arthrogryposis multiplex congenita (disorder)
synonymsCongenital muscular dystrophy with arthrogryposis multiplex congenita
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyDystrophy   4720007
Finding siteSkeletal muscle structure   127954009
attributes - group2
Clinical courseProgressive   255314001
attributes - group3
InterpretsRange of joint movement   364564000
Has interpretationDecreased   1250004
attributes - group4
Finding siteStructure of joint region   785818007
Associated morphologyContracture   57048009
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
parents
  • Congenital hereditary muscular dystrophy   111501005
  • Arthrogryposis multiplex congenita   205402004
  • Inherited arthrogryposis   28204005
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
          Congenital anomaly of skeletal muscle   89886004
            Congenital hereditary muscular dystrophy   111501005
              Congenital muscular dystrophy with arthrogryposis multiplex congenita   240061000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Deformity   417893002
      Congenital deformity   276655000
        Arthrogryposis   111246005
          Arthrogryposis multiplex congenita   205402004
            Congenital muscular dystrophy with arthrogryposis multiplex congenita   240061000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Inherited arthrogryposis   28204005
            Congenital muscular dystrophy with arthrogryposis multiplex congenita   240061000

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.