Trisomy 21- meiotic nondisjunction   205615000

SNOMED CT code


SNOMED code205615000
nameTrisomy 21- meiotic nondisjunction
statusactive
date introduced2002-01-31
fully specified name(s)Trisomy 21- meiotic nondisjunction (disorder)
synonymsTrisomy 21- meiotic nondisjunction
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyTrisomy   78989007
OccurrenceCongenital   255399007
Finding siteChromosome pair 21   43009003
parents
  • Whole chromosome trisomy meiotic nondisjunction   254269007
  • Complete trisomy 21 syndrome   41040004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Congenital chromosomal disease   74345006
          Trisomy and partial trisomy of autosome   270521004
            Whole chromosome trisomy meiotic nondisjunction   254269007
              Trisomy 21- meiotic nondisjunction   205615000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Complete trisomy 21 syndrome   41040004
            Trisomy 21- meiotic nondisjunction   205615000

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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