15q13.3 microdeletion 699254009
SNOMED CT code
SNOMED code | 699254009 |
---|---|
name | 15q13.3 microdeletion |
status | active |
date introduced | 2014-01-31 |
fully specified name(s) | Microdeletion of chromosome 15q13.3 (disorder) |
synonyms |
|
attributes - group1 | |
Finding site | Long arm of chromosome 312242007 |
Associated morphology | Partial monosomy 371169004 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Finding site | Chromosome pair 15 71678009 |
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 15 16569009 Deletion of part of chromosome 15 726386007 Partial deletion of long arm of chromosome 15 1162460001 15q13.3 microdeletion 699254009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 15q13.3 microdeletion 699254009 |
ancestors | sorted most to least specific
|
cpt crosswalks |
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