Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome 1187043002
SNOMED CT code
| SNOMED code | 1187043002 |
|---|---|
| name | Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome |
| status | active |
| date introduced | 2021-11-30 |
| fully specified name(s) | Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) |
| synonyms |
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| attributes - group2 | |
| Clinical course | Progressive 255314001 |
| attributes - group3 | |
| Finding site | Visual structure 49549006 |
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Central nervous system structure 21483005 |
| 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 Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome 1187043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome 1187043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic metabolic disorder 128289001 Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome 1187043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Disorder of eye movements 45030009 Strabismus 22066006 Oculomotor apraxia 193662007 Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome 1187043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome 1187043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of mineral metabolism 45744005 Disorder of trace mineral metabolism 15616006 Disorder of zinc metabolism 46727001 Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome 1187043002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome 1187043002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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