VACTERL syndrome with hydrocephalus   719043002

SNOMED CT code


SNOMED code719043002
nameVACTERL syndrome with hydrocephalus
statusactive
date introduced2017-01-31
fully specified name(s)Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus (disorder)
synonyms
  • Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-esophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
  • Vertebral abnormality, anal atresia, cardiac abnormality, tracheo-oesophageal fistula, renal anomaly, limb defect syndrome with hydrocephalus
  • VACTERL syndrome with hydrocephalus
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyDilatation   25322007
OccurrenceCongenital   255399007
Finding siteBrain cerebrospinal fluid pathway   280371009
parents
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of nervous system   363235000
  • Congenital hydrocephalus   47032000
  • Multiple system malformation syndrome   82354003
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          VACTERL syndrome with hydrocephalus   719043002

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
            VACTERL syndrome with hydrocephalus   719043002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Hydrocephalus   230745008
            Congenital hydrocephalus   47032000
              VACTERL syndrome with hydrocephalus   719043002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              VACTERL syndrome with hydrocephalus   719043002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              VACTERL syndrome with hydrocephalus   719043002

ancestors
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