Congenital keratoderma 6874009
SNOMED CT code
| SNOMED code | 6874009 |
|---|---|
| name | Congenital keratoderma |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Congenital keratoderma (disorder) |
| synonyms | Congenital keratoderma |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hyperkeratosis 26996000 |
| Finding site | Skin structure 39937001 |
| attributes - group2 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Keratinization 44138005 |
| parents | |
| children |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Disorder of keratinization 277905003 Inherited disorder of keratinization 254214009 Erythrokeratoderma 254215005 Congenital keratoderma 6874009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital keratoderma 6874009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Keratosis 254666005 Keratoderma 707209001 Congenital keratoderma 6874009 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Rough skin 816995008 Congenital keratoderma 6874009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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