SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Non dystrophic myotonia   424795008

SNOMED CT code


SNOMED code424795008
nameNon dystrophic myotonia
statusactive
date introduced2007-01-31
fully specified name(s)Non dystrophic myotonia (disorder)
synonymsNon dystrophic myotonia
attributes - group1
Finding siteSkeletal muscle structure   127954009
parents
  • Autosomal hereditary disorder   1899006
  • Myotonic disorder   193237003
  • Hereditary disorder of musculoskeletal system   363212003
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
            Non dystrophic myotonia   424795008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Muscle finding   106030000
      Disorder of muscle   129565002
        Disorder of skeletal muscle   75047002
          Myotonic disorder   193237003
            Non dystrophic myotonia   424795008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Non dystrophic myotonia   424795008

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

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