Ring chromosome 20 syndrome 23686004
SNOMED CT code
SNOMED code | 23686004 |
---|---|
name | Ring chromosome 20 syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Ring chromosome 20 syndrome (disorder) |
synonyms | Ring chromosome 20 syndrome |
attributes - group1 | |
Associated morphology | Ring chromosome 23345003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Chromosome pair 20 25610001 |
parents |
|
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Ring chromosome 1010276004 Ring chromosome 20 syndrome 23686004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Ring chromosome 20 syndrome 23686004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 20 9839007 Ring chromosome 20 syndrome 23686004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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