Gorlin syndrome 69408002
SNOMED CT code
| SNOMED code | 69408002 |
|---|---|
| name | Gorlin syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Gorlin syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Basal cell carcinoma in basal cell nevus syndrome 399569002 |
| 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 Gorlin syndrome 69408002 SNOMED CT Concept 138875005 Clinical finding 404684003 Mass of body structure 300848003 Neoplasm of integumentary system 400186008 Neoplasm of skin 126488004 Tumor of surface epithelium 254649008 Malignant tumor of surface epithelium 254650008 Basal cell carcinoma of skin 254701007 Gorlin syndrome 69408002 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Gorlin syndrome 69408002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Gorlin syndrome 69408002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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