FOXG1 syndrome   702450004

SNOMED CT code


SNOMED code702450004
nameFOXG1 syndrome
statusactive
date introduced2014-07-31
fully specified name(s)FOXG1 syndrome (disorder)
synonymsFOXG1 syndrome
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteBrain structure   12738006
OccurrenceCongenital   255399007
parents
  • Autosomal dominant hereditary disorder   11164009
  • Pervasive developmental disorder   35919005
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of nervous system   363235000
  • Congenital anomaly of brain   57148006
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
              FOXG1 syndrome   702450004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Mental disorder   74732009
        Developmental mental disorder   129104009
          Disorder of psychological development   192562009
            Pervasive developmental disorder   35919005
              FOXG1 syndrome   702450004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          FOXG1 syndrome   702450004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Hereditary disorder of nervous system   363235000
            FOXG1 syndrome   702450004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Congenital anomaly of central nervous system   128124001
          Congenital anomaly of brain   57148006
            FOXG1 syndrome   702450004

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.