19q13.11 microdeletion syndrome 719599008
SNOMED CT code
| SNOMED code | 719599008 |
|---|---|
| name | 19q13.11 microdeletion syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | 19q13.11 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group1 | |
| Finding site | Chromosome pair 19 89959003 |
| Associated morphology | Deletion of long arm 64329008 |
| Occurrence | Congenital 255399007 |
| attributes - group4 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group5 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group2 | |
| Associated morphology | Partial monosomy 371169004 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 19 89959003 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 19q13.11 microdeletion syndrome 719599008 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 19 79656000 Deletion of part of chromosome 19 726392001 Deletion of long arm of chromosome 19 726393006 19q13.11 microdeletion syndrome 719599008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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