Familial generalized lentiginosis 765195000
SNOMED CT code
| SNOMED code | 765195000 |
|---|---|
| name | Familial generalized lentiginosis |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Familial generalized lentiginosis (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skin structure 39937001 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Lentigo 767376003 |
| 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 Familial generalized lentiginosis 765195000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Congenital pigmentary skin anomalies 205564003 Familial generalized lentiginosis 765195000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Familial generalized lentiginosis 765195000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hamartoma 399960008 Congenital hamartoma of skin 400083002 Familial generalized lentiginosis 765195000 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Lentiginosis 402624000 Familial generalized lentiginosis 765195000 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Hereditary hypermelanosis 403804008 Familial generalized lentiginosis 765195000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital melanosis 86042009 Familial generalized lentiginosis 765195000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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