SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Autosomal dominant muscular dystrophy with limb girdle distribution  240067001

Autosomal dominant muscular dystrophy with gene located at 5q31  240068006

Late onset proximal muscular dystrophy with dysarthria   240069003

SNOMED CT code


SNOMED code240069003
nameLate onset proximal muscular dystrophy with dysarthria
statusactive
date introduced2002-01-31
fully specified name(s)Late onset proximal muscular dystrophy with dysarthria (disorder)
synonyms
  • Gilchrist type muscular dystrophy
  • Late onset proximal muscular dystrophy with dysarthria
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyDystrophy   4720007
Finding siteSkeletal muscle structure   127954009
attributes - group2
Clinical courseProgressive   255314001
parentsAutosomal dominant muscular dystrophy with gene located at 5q31   240068006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Autosomal dominant muscular dystrophy with limb girdle distribution   240067001
                Autosomal dominant muscular dystrophy with gene located at 5q31   240068006
                  Late onset proximal muscular dystrophy with dysarthria   240069003

ancestors
sorted most to least specific
  • Autosomal dominant muscular dystrophy with gene located at 5q31   240068006
  • Autosomal dominant muscular dystrophy with limb girdle distribution   240067001
  • Autosomal dominant hereditary disorder   11164009
  • Muscular dystrophy with predominantly proximal limb girdle distribution   240046001
  • Autosomal hereditary disorder   1899006
  • Hereditary progressive muscular dystrophy   193225000
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Muscular dystrophy   73297009
  • Hereditary disorder by system   363137000
  • Chronic disease of musculoskeletal system   128237006
  • Developmental disorder   5294002
  • Degenerative disorder of muscle   363058009
  • Degenerative disorder of musculoskeletal system   363059001
  • Disorder of skeletal muscle   75047002
  • Hereditary disease   32895009
  • Chronic disease   27624003
  • Disorder of musculoskeletal system   928000
  • Disorder of muscle   129565002
  • Degenerative disorder   362975008
  • Disorder of soft tissue   19660004
  • Genetic disease   782964007
  • Musculoskeletal finding   106028002
  • Disorder of body system   362965005
  • Muscle finding   106030000
  • General finding of soft tissue   248402002
  • 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.

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  • CPT® to SNOMED Crosswalks

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