Ring chromosome 7 syndrome 765489006
SNOMED CT code
| SNOMED code | 765489006 |
|---|---|
| name | Ring chromosome 7 syndrome |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Ring chromosome 7 syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 7 70488008 |
| Associated morphology | Ring chromosome 23345003 |
| Occurrence | Congenital 255399007 |
| 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 7 syndrome 765489006 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 7 37367006 Ring chromosome 7 syndrome 765489006 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 7 syndrome 765489006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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