Lethal arteriopathy syndrome due to fibulin-4 deficiency   782773005

SNOMED CT code


SNOMED code782773005
nameLethal arteriopathy syndrome due to fibulin-4 deficiency
statusactive
date introduced2019-07-31
fully specified name(s)Lethal arteriopathy syndrome due to fibulin-4 deficiency (disorder)
synonymsLethal arteriopathy syndrome due to fibulin-4 deficiency
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyAneurysm   85659009
Finding siteArterial structure   51114001
OccurrenceCongenital   255399007
parents
  • Congenital arterial aneurysm   282036005
  • Cardiovascular system hereditary disorder   363005004
  • Developmental hereditary disorder   363070008
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    General finding of soft tissue   248402002
      Disorder of soft tissue   19660004
        Soft tissue lesion   239953001
          Arterial aneurysm   233981004
            Congenital arterial aneurysm   282036005
              Lethal arteriopathy syndrome due to fibulin-4 deficiency   782773005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cardiovascular system hereditary disorder   363005004
          Lethal arteriopathy syndrome due to fibulin-4 deficiency   782773005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Lethal arteriopathy syndrome due to fibulin-4 deficiency   782773005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Lethal arteriopathy syndrome due to fibulin-4 deficiency   782773005

ancestors
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