Septo-optic dysplasia sequence   7611002

SNOMED CT code


SNOMED code7611002
nameSepto-optic dysplasia sequence
statusactive
date introduced2002-01-31
fully specified name(s)Septo-optic dysplasia sequence (disorder)
synonyms
  • Septo-optic dysplasia sequence
  • Septo optic dysplasia
  • De Morsier syndrome
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyHypoplasia   55199003
Finding sitePituitary structure   56329008
OccurrenceCongenital   255399007
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyHypoplasia   55199003
Finding siteOptic disc structure   81016008
OccurrenceCongenital   255399007
parents
  • Hypoplasia of optic disc   373650004
  • Congenital anomaly of pituitary gland   74012004
  • Hypopituitarism   74728003
  • Multiple system malformation syndrome   82354003
  • Congenital hypoplasia of cerebrum   93249003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Optic disc finding   247201009
        Optic disc disorder   128331005
          Congenital anomaly of optic disc   60505005
            Hypoplasia of optic disc   373650004
              Septo-optic dysplasia sequence   7611002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Disorder of pituitary gland   399244003
            Congenital anomaly of pituitary gland   74012004
              Septo-optic dysplasia sequence   7611002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Disorder of pituitary gland   399244003
            Hypopituitarism   74728003
              Septo-optic dysplasia sequence   7611002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Septo-optic dysplasia sequence   7611002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Congenital anomaly of central nervous system   128124001
          Congenital anomaly of brain   57148006
            Congenital anomaly of cerebrum   702628006
              Congenital hypoplasia of cerebrum   93249003
                Septo-optic dysplasia sequence   7611002

ancestors
sorted most to least specific
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