Multiple lentigines syndrome 111306001
SNOMED CT code
| SNOMED code | 111306001 |
|---|---|
| name | Multiple lentigines syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Multiple lentigines syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skin structure 39937001 |
| attributes - group2 | |
| Associated morphology | Lentigo 767376003 |
| Finding site | Structure of skin and/or mucous membrane 707862002 |
| parents | |
| 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 Multiple lentigines syndrome 111306001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Multiple lentigines syndrome 111306001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Multiple lentigines syndrome 111306001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Multiple lentigines syndrome 111306001 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Lentiginosis 402624000 Multiple lentigines syndrome 111306001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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