SNOMED CT Concept  138875005

Clinical finding  404684003

Central nervous system finding  246556002

Finding of brain  299718000

Seizure  91175000

Seizure disorder  128613002

Epilepsy  84757009

Generalized epilepsy  19598007

Genetic generalized epilepsy  1260407007

Myoclonic epilepsy in infancy   192990004

SNOMED CT code


SNOMED code192990004
nameMyoclonic epilepsy in infancy
statusactive
date introduced2002-01-31
fully specified name(s)Myoclonic epilepsy in infancy (disorder)
synonyms
  • Benign myoclonic epilepsy in infancy
  • Myoclonic epilepsy in infancy
  • MEI - myoclonic epilepsy in infancy
attributes - group1
Finding siteBrain structure   12738006
parentsGenetic generalized epilepsy   1260407007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Seizure   91175000
          Seizure disorder   128613002
            Epilepsy   84757009
              Generalized epilepsy   19598007
                Genetic generalized epilepsy   1260407007
                  Myoclonic epilepsy in infancy   192990004

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:
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