Pierre Robin sequence faciodigital anomaly syndrome 723461007
SNOMED CT code
SNOMED code | 723461007 |
---|---|
name | Pierre Robin sequence faciodigital anomaly syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Pierre Robin sequence faciodigital anomaly syndrome (disorder) |
synonyms |
|
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Face structure 89545001 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Finding site | Digit structure 82680008 |
parents |
|
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 Pierre Robin sequence faciodigital anomaly syndrome 723461007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Pierre Robin sequence faciodigital anomaly syndrome 723461007 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Disorder of digit 128597007 Congenital anomaly of digit 403855001 Pierre Robin sequence faciodigital anomaly syndrome 723461007 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 Robin sequence 4602007 Pierre Robin sequence faciodigital anomaly syndrome 723461007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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