Syndromic orbital border hypoplasia 717337001
SNOMED CT code
SNOMED code | 717337001 |
---|---|
name | Syndromic orbital border hypoplasia |
status | active |
date introduced | 2016-07-31 |
fully specified name(s) | Syndromic hypoplasia of orbital border (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Hypoplasia 55199003 |
Finding site | Orbital margin structure 77886003 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Finding site | Face structure 89545001 |
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 Syndromic orbital border hypoplasia 717337001 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Orbit finding 246912006 Orbital margin finding 246913001 Syndromic orbital border hypoplasia 717337001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Syndromic orbital border hypoplasia 717337001 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Syndromic orbital border hypoplasia 717337001 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Congenital anomaly of visual system 127329003 Congenital anomaly of orbit 54873004 Syndromic orbital border hypoplasia 717337001 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 Syndromic orbital border hypoplasia 717337001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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