Aicardi Goutieres syndrome type 3 1187047001
SNOMED CT code
| SNOMED code | 1187047001 |
|---|---|
| name | Aicardi Goutieres syndrome type 3 |
| status | active |
| date introduced | 2021-11-30 |
| fully specified name(s) | Aicardi Goutieres syndrome type 3 (disorder) |
| synonyms | Aicardi Goutieres syndrome type 3 |
| attributes - group1 | |
| Finding site | Basal ganglion structure 32610002 |
| Associated morphology | Pathologic calcification 18115005 |
| attributes - group2 | |
| Interprets | Movement 255324009 |
| attributes - group3 | |
| Interprets | Movement observable 363847004 |
| Has interpretation | Abnormal 263654008 |
| attributes - group4 | |
| Finding site | Myelinated nerve fiber structure 54115001 |
| Associated morphology | Myelin sheath alteration 125495003 |
| attributes - group5 | |
| Finding site | White matter structure of brain and spinal cord 389080008 |
| Associated morphology | Dystrophy 4720007 |
| attributes - group6 | |
| Finding site | Immune system structure 116003000 |
| Associated morphology | Inflammatory morphology 409774005 |
| Pathological process | Abnormal immune process 769247005 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Neurological lesion 299735001 Leukodystrophy 192781003 Aicardi Goutieres syndrome 230312006 Aicardi Goutieres syndrome type 3 1187047001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Aicardi Goutieres syndrome type 3 1187047001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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