Sialidosis 38795005
SNOMED CT code
| SNOMED code | 38795005 |
|---|---|
| name | Sialidosis |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Sialidosis (disorder) |
| synonyms |
|
| attributes - group3 | |
| Interprets | Movement 255324009 |
| attributes - group2 | |
| Finding site | Nervous system structure 25087005 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents |
|
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Disorder of lysosomal enzyme 23585005 Oligosaccharidosis 1155842003 Sialidosis 38795005 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Myoclonic disorder 127324008 Sialidosis 38795005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited metabolic disorder of nervous system 128190004 Sialidosis 38795005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Disorder of lysosomal enzyme 23585005 Mucolipidosis 70528007 Sialidosis 38795005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Sialidosis 38795005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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