Weber-Cockayne syndrome 294705005
SNOMED CT code
SNOMED code | 294705005 |
---|---|
name | Weber-Cockayne syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Dominant epidermolysis bullosa simplex, Weber-Cockayne type (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Epidermolysis 85269007 |
Finding site | Skin structure 39937001 |
parents | Autosomal dominant epidermolysis bullosa simplex 398170002 |
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 Autosomal dominant epidermolysis bullosa simplex 398170002 Weber-Cockayne syndrome 294705005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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