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

Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein  240055003

Severe autosomal recessive muscular dystrophy of childhood - North African type   240056002

SNOMED CT code


SNOMED code240056002
nameSevere autosomal recessive muscular dystrophy of childhood - North African type
statusremoved
date introduced2002-01-31
date removed2020-01-31
fully specified name(s)Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
synonymsSevere autosomal recessive muscular dystrophy of childhood - North African type
parentsAutosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein   240055003
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
              Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein   240055003
                Severe autosomal recessive muscular dystrophy of childhood - North African type   240056002  removed: 2020-01-31

ancestors
sorted most to least specific
  • Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein   240055003
  • Congenital hereditary muscular dystrophy   111501005
  • Autosomal recessive muscular dystrophy with limb girdle distribution   240054004
  • Muscular dystrophy with predominantly proximal limb girdle distribution   240046001
  • Congenital anomaly of skeletal muscle   89886004
  • Autosomal recessive hereditary disorder   85995004
  • Hereditary progressive muscular dystrophy   193225000
  • Autosomal hereditary disorder   1899006
  • Congenital anomaly of muscle AND/OR tendon   79191007
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Muscular dystrophy   73297009
  • Congenital anomaly of musculoskeletal system   73573004
  • Disorder of skeletal muscle   75047002
  • Hereditary disorder by system   363137000
  • Chronic disease of musculoskeletal system   128237006
  • Congenital malformation   276654001
  • Degenerative disorder of muscle   363058009
  • Degenerative disorder of musculoskeletal system   363059001
  • Hereditary disease   32895009
  • Disorder of muscle   129565002
  • Chronic disease   27624003
  • Developmental disorder   5294002
  • Disorder of soft tissue   19660004
  • Disorder of musculoskeletal system   928000
  • Degenerative disorder   362975008
  • Congenital disease   66091009
  • Genetic disease   782964007
  • Muscle finding   106030000
  • General finding of soft tissue   248402002
  • Musculoskeletal finding   106028002
  • Disorder of body system   362965005
  • Disease   64572001
  • Clinical finding   404684003
  • SNOMED CT Concept   138875005
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

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