Congenital hereditary endothelial dystrophy type 2 417395001
SNOMED CT code
SNOMED code | 417395001 |
---|---|
name | Congenital hereditary endothelial dystrophy type 2 |
status | active |
date introduced | 2005-07-31 |
fully specified name(s) | Congenital hereditary endothelial dystrophy type 2 (disorder) |
synonyms |
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attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Chromosome pair 20 25610001 |
Associated morphology | Cellular AND/OR subcellular abnormality 107673000 |
attributes - group1 | |
Associated morphology | Dystrophy 4720007 |
Finding site | Structure of corneal endothelium 65431007 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital hereditary endothelial dystrophy 417651000 Congenital hereditary endothelial dystrophy type 2 417395001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital hereditary endothelial dystrophy type 2 417395001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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