Monosomy 21, mosaicism 205638002
SNOMED CT code
SNOMED code | 205638002 |
---|---|
name | Monosomy 21, mosaicism |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Monosomy 21, mosaicism (disorder) |
synonyms | Monosomy 21, mosaicism |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Cellular AND/OR subcellular abnormality 107673000 |
Finding site | Chromosome 91272006 |
parents | Monosomy and deletion from autosome 205627002 |
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 Monosomy and deletion from autosome 205627002 Monosomy 21, mosaicism 205638002 |
ancestors | sorted most to least specific |
cpt crosswalks |
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