Peutz-Jeghers syndrome 54411001
SNOMED CT code
| SNOMED code | 54411001 |
|---|---|
| name | Peutz-Jeghers syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Peutz-Jeghers syndrome (disorder) |
| synonyms |
|
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Neoplasm 108369006 |
| Finding site | Nervous system structure 25087005 |
| attributes - group4 | |
| Associated morphology | Neoplasm 108369006 |
| Finding site | Skin structure 39937001 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Structure of skin and/or mucous membrane 707862002 |
| Associated morphology | Lentigo 767376003 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Associated morphology | Peutz Jeghers polyp 277161008 |
| Finding site | Intestinal structure 113276009 |
| Occurrence | Congenital 255399007 |
| parents |
|
| children | Peutz-Jeghers polyps of small bowel 53633000 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Mass of digestive structure 300855001 Polyp of intestine 254588001 Intestinal polyposis syndrome 254589009 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Mass of digestive structure 300855001 Hamartoma of intestine 254594009 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hamartoma 399960008 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Lentiginosis 402624000 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Neurocutaneous syndrome 78572006 Peutz-Jeghers syndrome 54411001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital melanosis 86042009 Peutz-Jeghers syndrome 54411001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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