Paternal uniparental disomy of chromosome 13 770668007
SNOMED CT code
SNOMED code | 770668007 |
---|---|
name | Paternal uniparental disomy of chromosome 13 |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Paternal uniparental disomy of chromosome 13 (disorder) |
synonyms | Paternal uniparental disomy of chromosome 13 |
attributes - group1 | |
Finding site | Chromosome pair 13 55401003 |
Occurrence | Congenital 255399007 |
Associated morphology | Alteration of chromosome structure 41669009 |
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 13 17760001 Paternal uniparental disomy of chromosome 13 770668007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Uniparental disomy 726400003 Uniparental disomy of paternal origin 726402006 Paternal uniparental disomy of chromosome 13 770668007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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