17q23.1q23.2 microdeletion syndrome 719584008
SNOMED CT code
SNOMED code | 719584008 |
---|---|
name | 17q23.1q23.2 microdeletion syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | 17q23.1q23.2 microdeletion syndrome (disorder) |
synonyms | 17q23.1q23.2 microdeletion syndrome |
attributes - group2 | |
Associated morphology | Partial monosomy 371169004 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Chromosome pair 17 45201007 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Long arm of chromosome 312242007 |
Associated morphology | Partial monosomy 371169004 |
Pathological process | Pathological developmental process 308490002 |
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 17 32107005 Deletion of part of chromosome 17 726389000 Deletion of part of long arm of chromosome 17 733300002 17q23.1q23.2 microdeletion syndrome 719584008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 17q23.1q23.2 microdeletion syndrome 719584008 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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