Trisomy 21- meiotic nondisjunction 205615000
SNOMED CT code
SNOMED code | 205615000 |
---|---|
name | Trisomy 21- meiotic nondisjunction |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Trisomy 21- meiotic nondisjunction (disorder) |
synonyms | Trisomy 21- meiotic nondisjunction |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Trisomy 78989007 |
Occurrence | Congenital 255399007 |
Finding site | Chromosome pair 21 43009003 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Trisomy and partial trisomy of autosome 270521004 Whole chromosome trisomy meiotic nondisjunction 254269007 Trisomy 21- meiotic nondisjunction 205615000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Complete trisomy 21 syndrome 41040004 Trisomy 21- meiotic nondisjunction 205615000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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