Isotretinoin-like syndrome 722006004
SNOMED CT code
| SNOMED code | 722006004 |
|---|---|
| name | Isotretinoin-like syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Isotretinoin embryopathy-like syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Aortic arch structure 57034009 |
| attributes - group3 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Face structure 89545001 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Central nervous system structure 21483005 |
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Congenital smallness 41086002 |
| Finding site | External ear structure 28347008 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Isotretinoin-like syndrome 722006004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Congenital malformation of ear 275259005 Congenital abnormality of external ear 282038006 Microtia 35045004 Isotretinoin-like syndrome 722006004 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Isotretinoin-like syndrome 722006004 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Isotretinoin-like syndrome 722006004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Isotretinoin-like syndrome 722006004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Isotretinoin-like syndrome 722006004 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 Isotretinoin-like syndrome 722006004 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of trunk structure 302292003 Disorder of trunk 128121009 Disorder of aorta 47040006 Congenital anomaly of aorta 59877000 Congenital anomaly of aortic arch 79439001 Isotretinoin-like syndrome 722006004 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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