Epidermolysis bullosa simplex due to exophilin 5 deficiency 773503009
SNOMED CT code
SNOMED code | 773503009 |
---|---|
name | Epidermolysis bullosa simplex due to exophilin 5 deficiency |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Epidermolysis bullosa simplex due to exophilin 5 deficiency (disorder) |
synonyms | Epidermolysis bullosa simplex due to exophilin 5 deficiency |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Skin structure 39937001 |
Associated morphology | Epidermolysis 85269007 |
parents | Autosomal recessive epidermolysis bullosa simplex 1156849001 |
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 recessive hereditary disorder 85995004 Autosomal recessive epidermolysis bullosa simplex 1156849001 Epidermolysis bullosa simplex due to exophilin 5 deficiency 773503009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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