Trisomy 10p   717157006

SNOMED CT code


SNOMED code717157006
nameTrisomy 10p
statusactive
date introduced2016-07-31
fully specified name(s)Trisomy 10p (disorder)
synonymsTrisomy 10p
attributes - group2
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteFace structure   89545001
attributes - group1
OccurrenceCongenital   255399007
Finding siteChromosome pair 10   56332006
Associated morphologyTrisomy   78989007
Pathological processPathological developmental process   308490002
attributes - group3
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteLimb structure   66019005
attributes - group4
InterpretsIntellectual ability   247573007
Has interpretationImpaired   260379002
attributes - group5
InterpretsAdaptation behavior   406208005
Has interpretationImpaired   260379002
parents
  • Intellectual disability   110359009
  • Trisomy 10   205651007
  • Multiple malformation syndrome with facial-limb defects as major feature   23359005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Mental state, behavior and/or psychosocial function finding   384821006
      Behavior finding   844005
        Intellectual disability   110359009
          Trisomy 10p   717157006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chromosomal disorder   409709004
        Congenital chromosomal disease   74345006
          Trisomy and partial trisomy of autosome   270521004
            Trisomy 10   205651007
              Trisomy 10p   717157006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Congenital anomaly of limb   60475009
          Multiple malformation syndrome with facial-limb defects as major feature   23359005
            Trisomy 10p   717157006

ancestors
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cpt crosswalks

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