Fragile X chromosome 205720009
SNOMED CT code
SNOMED code | 205720009 |
---|---|
name | Fragile X chromosome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Fragile X chromosome (disorder) |
synonyms | Fragile X chromosome |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Associated morphology | Chromosomal morphology 107675007 |
Finding site | Sex chromosome X 72837006 |
parents | Anomaly of chromosome X 111312006 |
children | |
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 sex chromosome 95462004 Anomaly of chromosome X 111312006 Fragile X chromosome 205720009 |
ancestors | sorted most to least specific |
cpt crosswalks |
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