SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital atrophy of optic nerve   722990003

SNOMED CT code


SNOMED code722990003
nameCongenital atrophy of optic nerve
statusactive
date introduced2017-01-31
fully specified name(s)Congenital atrophy of optic nerve (disorder)
synonyms
  • Congenital atrophy of optic nerve
  • Congenital optic atrophy
attributes - group1
Associated morphologyAtrophy   13331008
OccurrenceCongenital   255399007
Finding siteOptic nerve structure   18234004
parents
children
  • CAMOS syndrome   726031001
  • Combined immunodeficiency with faciooculoskeletal anomalies syndrome   770625006
  • Early-onset X-linked optic atrophy   721200000
  • Late congenital syphilitic optic atrophy   1142031005
  • Leber plus disease   719430008
  • Severe X-linked intellectual disability Gustavson type   722213009
  • Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome   1237618009
  • Wolfram-like syndrome   734022008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital atrophy of optic nerve   722990003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Degenerative disease of the central nervous system   80690008
          Optic atrophy   76976005
            Congenital atrophy of optic nerve   722990003

ancestors
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