Polymicrogyria with optic nerve hypoplasia 771336003
SNOMED CT code
| SNOMED code | 771336003 |
|---|---|
| name | Polymicrogyria with optic nerve hypoplasia |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Polymicrogyria with optic nerve hypoplasia (disorder) |
| synonyms | Polymicrogyria with optic nerve hypoplasia |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Congenital smallness 41086002 |
| Finding site | Gyrus of brain 3964001 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Optic nerve structure 18234004 |
| Associated morphology | Hypoplasia 55199003 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group4 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Polymicrogyria with optic nerve hypoplasia 771336003 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 Polymicrogyria with optic nerve hypoplasia 771336003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Polymicrogyria with optic nerve hypoplasia 771336003 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 Disorder of neuronal migration and differentiation 253146009 Microgyria 4945003 Bilateral polymicrogyria 765757003 Polymicrogyria with optic nerve hypoplasia 771336003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Polymicrogyria with optic nerve hypoplasia 771336003 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of optic nerve 95502000 Hypoplasia of the optic nerve 95499004 Polymicrogyria with optic nerve hypoplasia 771336003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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