Microphthalmia with brain atrophy syndrome 720010009
SNOMED CT code
| SNOMED code | 720010009 |
|---|---|
| name | Microphthalmia with brain atrophy syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Microphthalmia with brain atrophy syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Brain structure 12738006 |
| Associated morphology | Atrophy 13331008 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Congenital smallness 41086002 |
| Occurrence | Congenital 255399007 |
| Finding site | Entire eye proper 1290040004 |
| 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 Microphthalmia with brain atrophy syndrome 720010009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Microphthalmia with brain atrophy syndrome 720010009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Microphthalmia with brain atrophy syndrome 720010009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Degenerative brain disorder 52522001 Microphthalmia with brain atrophy syndrome 720010009 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 with brain atrophy syndrome 720010009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Microphthalmia with brain atrophy syndrome 720010009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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