Crome syndrome   722381004

SNOMED CT code


SNOMED code722381004
nameCrome syndrome
statusactive
date introduced2017-01-31
fully specified name(s)Congenital cataract, nephropathy, encephalopathy syndrome (disorder)
synonyms
  • Congenital cataract, nephropathy, encephalopathy syndrome
  • Crome syndrome
attributes - group3
Pathological processPathological developmental process   308490002
Associated morphologyOpacity   128305008
OccurrenceCongenital   255399007
Finding siteLens clear   78076003
attributes - group2
Pathological processPathological developmental process   308490002
Finding siteBrain structure   12738006
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteRenal tubule structure   58471003
Associated morphologyNecrosis   6574001
attributes - group4
InterpretsHeight / growth measure   271603002
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Traumatic or nontraumatic brain injury   127294003
            Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of general physiological development   271616002
      Disorder of stature   237834000
        Short stature disorder   237836003
          Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of sensory organ   1279550006
        Disorder of eye   371405004
          Injury of globe of eye   231794000
            Injury of lens   262755005
              Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Crome syndrome   722381004

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
            Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Hereditary nephropathy   367591000119105
              Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Injury of internal organ   105612003
        Injury of kidney   40095003
          Renal cortical necrosis   444691002
            Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Congenital anomaly of the kidney   44513007
              Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disorder of eye   62585004
          Cataract   193570009
            Congenital cataract   79410001
              Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Crome syndrome   722381004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Disorder of renal parenchyma   767094002
              Renal tubular disorder   95568003
                Crome syndrome   722381004

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