15q11q13 microduplication syndrome 719427001
SNOMED CT code
| SNOMED code | 719427001 |
|---|---|
| name | 15q11q13 microduplication syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | 15q11q13 microduplication syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Long arm of chromosome 312242007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Partial trisomy 133849008 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 15 71678009 |
| Associated morphology | Partial trisomy 133849008 |
| Pathological process | Pathological developmental process 308490002 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Trisomy and partial trisomy of autosome 270521004 Partial trisomy of chromosome 15 726354002 Partial duplication of long arm of chromosome 15 1162463004 15q11q13 microduplication syndrome 719427001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 15q11q13 microduplication syndrome 719427001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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