Whole chromosome monosomy - meiotic nondisjunction 205636003
SNOMED CT code
SNOMED code | 205636003 |
---|---|
name | Whole chromosome monosomy - meiotic nondisjunction |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Whole chromosome monosomy - meiotic nondisjunction (disorder) |
synonyms | Whole chromosome monosomy - meiotic nondisjunction |
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 Whole chromosome monosomy - meiotic nondisjunction 205636003 |
ancestors | sorted most to least specific |
cpt crosswalks |
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