Ovarioleukodystrophy 1156768008
SNOMED CT code
| SNOMED code | 1156768008 |
|---|---|
| name | Ovarioleukodystrophy |
| status | active |
| date introduced | 2021-07-31 |
| fully specified name(s) | Ovarioleukodystrophy (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Myelin sheath alteration 125495003 |
| Finding site | Myelinated nerve fiber structure 54115001 |
| attributes - group3 | |
| Interprets | Hormone secretion 60877009 |
| Has interpretation | Decreased 1250004 |
| attributes - group2 | |
| Finding site | Cerebral white matter structure 68523003 |
| Associated morphology | Dystrophy 4720007 |
| attributes - group4 | |
| Finding site | Ovarian endocrine structure 304043001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Endocrine finding 106176003 Decreased hormone secretion 42497006 Ovarian failure 111550004 Primary ovarian failure 65846009 Premature ovarian failure 237788002 Ovarioleukodystrophy 1156768008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Ovarioleukodystrophy 1156768008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 Ovarioleukodystrophy 1156768008 SNOMED CT Concept 138875005 Clinical finding 404684003 Neurological lesion 299735001 Leukodystrophy 192781003 Vanishing white matter disease 447351004 Ovarioleukodystrophy 1156768008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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