Gastrocutaneous syndrome 782946000
SNOMED CT code
| SNOMED code | 782946000 |
|---|---|
| name | Gastrocutaneous syndrome |
| status | active |
| date introduced | 2019-07-31 |
| fully specified name(s) | Gastrocutaneous syndrome (disorder) |
| synonyms | Gastrocutaneous syndrome |
| attributes - group1 | |
| Finding site | Skin structure 39937001 |
| Associated morphology | Hyperpigmentation 4830009 |
| attributes - group2 | |
| Finding site | Upper gastrointestinal tract structure 62834003 |
| 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 Gastrocutaneous syndrome 782946000 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Gastrointestinal tract finding 386618008 Disorder of gastrointestinal tract 119292006 Disorder of upper gastrointestinal tract 119291004 Gastrocutaneous syndrome 782946000 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Gastrocutaneous syndrome 782946000 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Gastrocutaneous syndrome 782946000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Hyperpigmentation of skin 49765009 Gastrocutaneous syndrome 782946000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Gastrocutaneous syndrome 782946000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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