Atypical Rett syndrome   718393002

SNOMED CT code


SNOMED code718393002
nameAtypical Rett syndrome
statusactive
date introduced2016-07-31
fully specified name(s)Atypical Rett syndrome (disorder)
synonymsAtypical Rett syndrome
attributes - group1
Pathological processPathological developmental process   308490002
parents
  • X-linked hereditary disease   128430005
  • Pervasive developmental disorder   35919005
  • Developmental hereditary disorder   363070008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              Atypical Rett syndrome   718393002

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
              Atypical Rett syndrome   718393002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Atypical Rett syndrome   718393002

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.