49,XXXYY syndrome 770908007
SNOMED CT code
SNOMED code | 770908007 |
---|---|
name | 49,XXXYY syndrome |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | 49,XXXYY syndrome (disorder) |
synonyms | 49,XXXYY syndrome |
attributes - group1 | |
Finding site | Sex chromosome Y 5421003 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Aneuploidy 80056000 |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Sex chromosome X 72837006 |
Associated morphology | Aneuploidy 80056000 |
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 sex chromosome 95462004 Anomaly of chromosome X 111312006 49,XXXYY syndrome 770908007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of sex chromosome 95462004 Sex chromosome aneuploidy 725084009 49,XXXYY syndrome 770908007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of sex chromosome 95462004 Anomaly of chromosome Y 81438002 49,XXXYY syndrome 770908007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 49,XXXYY syndrome 770908007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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