Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002
SNOMED CT code
| SNOMED code | 778021002 |
|---|---|
| name | Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome (disorder) |
| synonyms |
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| attributes - group4 | |
| Finding site | Retinal structure 5665001 |
| Associated morphology | Dystrophy 4720007 |
| attributes - group1 | |
| Associated morphology | Hyaline body 18695008 |
| Finding site | Optic disc structure 81016008 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Congenital smallness 41086002 |
| Finding site | Entire eye proper 1290040004 |
| attributes - group3 | |
| Associated morphology | Separation 16640008 |
| Finding site | Structure of fovea centralis 67046006 |
| parents |
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| 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 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Optic disc finding 247201009 Optic disc disorder 128331005 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 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 retinitis pigmentosa 232053004 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 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 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Retina finding 399858007 Macula finding 247143009 Macular disorder 312999006 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Optic disc finding 247201009 Drusen of optic disc 33629003 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disorder of eye 62585004 Degeneration of retina 95695004 Retinoschisis 44268007 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of eye 19416009 Microphthalmos 61142002 Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome 778021002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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