Autosomal recessive isolated optic atrophy 1197151003
SNOMED CT code
| SNOMED code | 1197151003 |
|---|---|
| name | Autosomal recessive isolated optic atrophy |
| status | active |
| date introduced | 2022-02-28 |
| fully specified name(s) | Autosomal recessive isolated optic atrophy (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Structure of left optic nerve 724379002 |
| Associated morphology | Atrophy 13331008 |
| attributes - group2 | |
| Finding site | Structure of right optic nerve 724380004 |
| Associated morphology | Atrophy 13331008 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Hereditary degenerative disease of central nervous system 106018006 Autosomal recessive isolated optic atrophy 1197151003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Optic atrophy 76976005 Optic atrophy of right eye 15632811000119100 Bilateral optic atrophy of eyes 15632891000119109 Autosomal recessive isolated optic atrophy 1197151003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Inherited optic neuropathy 312942003 Autosomal recessive isolated optic atrophy 1197151003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive isolated optic atrophy 1197151003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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