RIDDLE syndrome 783099001
SNOMED CT code
SNOMED code | 783099001 |
---|---|
name | RIDDLE syndrome |
status | active |
date introduced | 2019-07-31 |
fully specified name(s) | Radiosensitivity, immunodeficiency, dysmorphic features, learning difficulties syndrome (disorder) |
synonyms |
|
attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Face structure 89545001 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Pathological process | Abnormal immune process 769247005 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 RIDDLE syndrome 783099001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 RIDDLE syndrome 783099001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Combined immunodeficiency disease 442459007 RIDDLE syndrome 783099001 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 RIDDLE syndrome 783099001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 RIDDLE syndrome 783099001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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