16q24.1 microdeletion syndrome 770760006
SNOMED CT code
| SNOMED code | 770760006 |
|---|---|
| name | 16q24.1 microdeletion syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | 16q24.1 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Long arm of chromosome 312242007 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Partial monosomy 371169004 |
| attributes - group2 | |
| Associated morphology | Partial monosomy 371169004 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 16 39220001 |
| attributes - group3 | |
| Finding site | Structure of interstitial tissue of lung 113254000 |
| 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 16 53392002 Deletion of part of chromosome 16 726387003 Partial deletion of long arm of chromosome 16 1162478006 16q24.1 microdeletion syndrome 770760006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Interstitial lung disease 233703007 16q24.1 microdeletion syndrome 770760006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 16q24.1 microdeletion syndrome 770760006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Congenital connective tissue disorder 363039000 16q24.1 microdeletion syndrome 770760006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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