Erythrokeratodermia variabilis 70041004
SNOMED CT code
SNOMED code | 70041004 |
---|---|
name | Erythrokeratodermia variabilis |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Erythrokeratodermia variabilis (disorder) |
synonyms |
|
attributes - group1 | |
Finding site | Entire skin 181469002 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Hyperkeratosis 26996000 |
attributes - group2 | |
Has interpretation | Abnormal 263654008 |
Interprets | Keratinization 44138005 |
parents | |
children | Malignant atrophic papulosis 11131009 removed: 2003-07-31 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Rough skin 816995008 Congenital ichthyosis of skin 13059002 Erythrokeratodermia variabilis 70041004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Erythrokeratodermia variabilis 70041004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital keratoderma 6874009 Erythrokeratodermia variabilis 70041004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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