Genitopalatocardiac syndrome   773749003

SNOMED CT code


SNOMED code773749003
nameGenitopalatocardiac syndrome
statusactive
date introduced2019-01-31
fully specified name(s)Genitopalatocardiac syndrome (disorder)
synonyms
  • Genitopalatocardiac syndrome
  • Gardner Silengo Wachtel syndrome
attributes - group2
Associated morphologyDevelopmental failure of fusion   371520008
Pathological processPathological developmental process   308490002
Finding sitePalatal structure   72914001
OccurrenceCongenital   255399007
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteGonadal structure   43174007
Associated morphologyMorphologically abnormal structure   49755003
attributes - group3
Finding siteHeart structure   80891009
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
parents
  • Congenital heart disease   13213009
  • Cardiovascular system hereditary disorder   363005004
  • Reproductive system hereditary disorder   363290007
  • Multiple system malformation syndrome   82354003
  • Autosomal recessive hereditary disorder   85995004
  • Cleft palate   87979003
  • Pure gonadal dysgenesis 46,XY   95218005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Cardiovascular finding   106063007
        Cardiac finding   301095005
          Heart disease   56265001
            Structural disorder of heart   128599005
              Congenital heart disease   13213009
                Genitopalatocardiac syndrome   773749003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Cardiovascular finding   106063007
        Disorder of cardiovascular system   49601007
          Cardiovascular system hereditary disorder   363005004
            Genitopalatocardiac syndrome   773749003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary disorder by system   363137000
            Reproductive system hereditary disorder   363290007
              Genitopalatocardiac syndrome   773749003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Genitopalatocardiac syndrome   773749003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Genitopalatocardiac syndrome   773749003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of head   118934005
          Disorder of palate   128337009
            Congenital anomaly of palate   128336000
              Cleft palate   87979003
                Genitopalatocardiac syndrome   773749003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Congenital abnormality of lower limb and pelvic girdle   253937004
          Congenital anomaly of lower trunk   363030001
            Genitourinary congenital anomalies   287085006
              Congenital malformation of genital organs   204821009
                Gonadal dysgenesis   205681004
                  Pure gonadal dysgenesis   95219002
                    Pure gonadal dysgenesis 46,XY   95218005
                      Genitopalatocardiac syndrome   773749003

ancestors
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