Illum syndrome 720514008
SNOMED CT code
SNOMED code | 720514008 |
---|---|
name | Illum syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Arthrogryposis multiplex congenita and whistling face syndrome (disorder) |
synonyms |
|
attributes - group2 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Contracture 57048009 |
Finding site | Structure of joint region 785818007 |
attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Face structure 89545001 |
attributes - group3 | |
Interprets | Range of joint movement 364564000 |
Has interpretation | Decreased 1250004 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Deformity 417893002 Congenital deformity 276655000 Arthrogryposis 111246005 Arthrogryposis multiplex congenita 205402004 Illum syndrome 720514008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Inherited arthrogryposis 28204005 Illum syndrome 720514008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Illum syndrome 720514008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Illum syndrome 720514008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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