Chromosomal alterations of group F 123651000
SNOMED CT code
SNOMED code | 123651000 |
---|---|
name | Chromosomal alterations of group F |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Chromosomal alterations of group F (disorder) |
synonyms | Chromosomal alterations of group F |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Morphologically abnormal structure 49755003 |
Finding site | Chromosomes, group F 74099009 |
parents | Group chromosomal alteration 123645005 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Group chromosomal alteration 123645005 Chromosomal alterations of group F 123651000 |
ancestors | sorted most to least specific |
cpt crosswalks |
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