Autosomal dominant epidermolysis bullosa simplex 398170002
SNOMED CT code
SNOMED code | 398170002 |
---|---|
name | Autosomal dominant epidermolysis bullosa simplex |
status | active |
date introduced | 2003-07-31 |
fully specified name(s) | Autosomal dominant epidermolysis bullosa simplex (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Epidermolysis 85269007 |
Finding site | Skin structure 39937001 |
parents | |
children |
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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 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Epidermolysis bullosa 61003004 Epidermolysis bullosa simplex 67144006 Autosomal dominant epidermolysis bullosa simplex 398170002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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