15q11.2 microdeletion syndrome 771340007
SNOMED CT code
| SNOMED code | 771340007 |
|---|---|
| name | 15q11.2 microdeletion syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | 15q11.2 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Partial monosomy 371169004 |
| Finding site | Long arm of chromosome 312242007 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 15 71678009 |
| Associated morphology | Partial monosomy 371169004 |
| 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 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 15 16569009 Deletion of part of chromosome 15 726386007 Partial deletion of long arm of chromosome 15 1162460001 15q11.2 microdeletion syndrome 771340007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 15q11.2 microdeletion syndrome 771340007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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