Paternal uniparental disomy of chromosome 15 1003871005
SNOMED CT code
SNOMED code | 1003871005 |
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name | Paternal uniparental disomy of chromosome 15 |
status | active |
date introduced | 2021-01-31 |
fully specified name(s) | Uniparental disomy of paternal origin of chromosome 15 (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Alteration of chromosome structure 41669009 |
Finding site | Chromosome pair 15 71678009 |
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 Paternal uniparental disomy of chromosome 15 1003871005 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 15 1003871005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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