Eiken syndrome 720863002
SNOMED CT code
SNOMED code | 720863002 |
---|---|
name | Eiken syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Eiken syndrome (disorder) |
synonyms | Eiken syndrome |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Bone structure 272673000 |
Associated morphology | Demineralized structure 128420001 |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Structure of epiphysis 43719000 |
Associated morphology | Dysplasia 25723000 |
attributes - group3 | |
Clinical course | Progressive 255314001 |
attributes - group4 | |
Interprets | Height / growth measure 271603002 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disorder of musculoskeletal system 363059001 Degenerative disorder of bone 363054006 Osteopenia 312894000 Eiken syndrome 720863002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic disease of musculoskeletal system 128237006 Epiphyseal dysplasia 254080004 Multiple epiphyseal dysplasia 59708000 Eiken syndrome 720863002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Eiken syndrome 720863002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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