Prader-Willi syndrome 89392001
SNOMED CT code
| SNOMED code | 89392001 |
|---|---|
| name | Prader-Willi syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Prader-Willi syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of distal part of pituitary 52618001 |
| attributes - group1 | |
| Finding site | Gonadal endocrine structure 304041004 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Neurodevelopmental disorder 700364009 Prader-Willi syndrome 89392001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hypogonadotropic hypogonadism 722944006 Prader-Willi syndrome 89392001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Prader-Willi syndrome 89392001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Prader-Willi syndrome 89392001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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