Leber's optic atrophy 58610003
SNOMED CT code
| SNOMED code | 58610003 |
|---|---|
| name | Leber's optic atrophy |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Leber's optic atrophy (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Optic nerve structure 18234004 |
| Associated morphology | Primary atrophy 68616007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| parents |
|
| children | Leber plus disease 719430008 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Maternally inherited mitochondrial deoxyribonucleic acid disease 1162975000 Leber's optic atrophy 58610003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited metabolic disorder of nervous system 128190004 Leber's optic atrophy 58610003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of pyruvate metabolism and mitochondrial respiratory chain 237981000 Leber's optic atrophy 58610003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Mitochondrial cytopathy 240096000 Leber's optic atrophy 58610003 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 Hereditary optic atrophy 26360005 Leber's optic atrophy 58610003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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