7p21.1 deletion syndrome 890127007
SNOMED CT code
| SNOMED code | 890127007 |
|---|---|
| name | 7p21.1 deletion syndrome |
| status | active |
| date introduced | 2021-01-31 |
| fully specified name(s) | 7p21.1 deletion syndrome (disorder) |
| synonyms | 7p21.1 deletion syndrome |
| attributes - group1 | |
| Associated morphology | Partial monosomy 371169004 |
| Finding site | Chromosome pair 7 70488008 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Short arm of chromosome 278145009 |
| Associated morphology | Partial monosomy 371169004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 7 37367006 Deletion of part of chromosome 7 726377002 7p partial monosomy 24786004 7p21.1 deletion syndrome 890127007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 7p21.1 deletion syndrome 890127007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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