Cutis laxa, autosomal dominant 111388003
SNOMED CT code
SNOMED code | 111388003 |
---|---|
name | Cutis laxa, autosomal dominant |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Cutis laxa, autosomal dominant (disorder) |
synonyms | Cutis laxa, autosomal dominant |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Connective tissue structure 21793004 |
attributes - group2 | |
Finding site | Skin structure 39937001 |
parents | |
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 Cutis laxa, autosomal dominant 111388003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Congenital connective tissue disorder 363039000 Inherited cutis laxa 254220005 Cutis laxa, autosomal dominant 111388003 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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