7q31 microdeletion syndrome 773326003
SNOMED CT code
| SNOMED code | 773326003 |
|---|---|
| name | 7q31 microdeletion syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | 7q31 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Partial monosomy 371169004 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Long arm of chromosome 312242007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Partial monosomy 371169004 |
| Finding site | Chromosome pair 7 70488008 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 7q31 microdeletion syndrome 773326003 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 7 37367006 Deletion of part of chromosome 7 726377002 7q partial monosomy 81304006 7q31 microdeletion syndrome 773326003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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