Paternal 20q13.2q13.3 microdeletion syndrome 724070005
SNOMED CT code
| SNOMED code | 724070005 |
|---|---|
| name | Paternal 20q13.2q13.3 microdeletion syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Paternal 20q13.2q13.3 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Chromosome pair 20 25610001 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Partial monosomy 371169004 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Long arm of chromosome 312242007 |
| 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 20 9839007 Deletion of part of chromosome 20 726395004 Deletion of part of long arm of chromosome 20 726396003 Paternal 20q13.2q13.3 microdeletion syndrome 724070005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Paternal 20q13.2q13.3 microdeletion syndrome 724070005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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