8q22.1 microdeletion syndrome 719664004
SNOMED CT code
| SNOMED code | 719664004 |
|---|---|
| name | 8q22.1 microdeletion syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | 8q22.1 microdeletion syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 8 77826001 |
| Associated morphology | Partial monosomy 371169004 |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Face structure 89545001 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Chromosome pair 8 77826001 |
| Associated morphology | Deletion of long arm 64329008 |
| 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 8 48082007 Deletion of part of chromosome 8 726378007 8q partial monosomy syndrome 29379007 8q22.1 microdeletion syndrome 719664004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 8q22.1 microdeletion syndrome 719664004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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