Ring chromosome 11 syndrome 111310003
SNOMED CT code
| SNOMED code | 111310003 |
|---|---|
| name | Ring chromosome 11 syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Ring chromosome 11 syndrome (disorder) |
| synonyms | Ring chromosome 11 syndrome |
| attributes - group1 | |
| Associated morphology | Ring chromosome 23345003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 11 16312006 |
| parents |
|
| children | Café-au-lait spots and ring chromosome 11 403758009 removed: 2021-07-31 |
| 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 11 syndrome 111310003 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 11 60891003 Ring chromosome 11 syndrome 111310003 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 11 syndrome 111310003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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