Legius syndrome 703541007
SNOMED CT code
| SNOMED code | 703541007 |
|---|---|
| name | Legius syndrome |
| status | active |
| date introduced | 2014-07-31 |
| fully specified name(s) | Neurofibromatosis type 1-like syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hyperpigmentation 4830009 |
| Finding site | Skin structure 39937001 |
| 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 Legius syndrome 703541007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Cafe-au-lait spots 201281002 Legius syndrome 703541007 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Legius syndrome 703541007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Hyperpigmentation of skin 49765009 Legius syndrome 703541007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Legius syndrome 703541007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Legius syndrome 703541007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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