SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Sex-linked hereditary disorder  82852009

X-linked hereditary disease  128430005

X-linked optic atrophy  1231634003

Early-onset X-linked optic atrophy   721200000

SNOMED CT code


SNOMED code721200000
nameEarly-onset X-linked optic atrophy
statusactive
date introduced2017-01-31
fully specified name(s)Early-onset X-linked optic atrophy (disorder)
synonyms
  • Early-onset X-linked optic atrophy
  • Non-Leber type optic atrophy with early-onset
  • Optic atrophy type 2
attributes - group2
Associated morphologyPrimary atrophy   68616007
OccurrenceCongenital   255399007
Finding siteOptic nerve structure   18234004
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              X-linked optic atrophy   1231634003
                Early-onset X-linked optic atrophy   721200000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital atrophy of optic nerve   722990003
          Early-onset X-linked optic atrophy   721200000

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