FRAXF syndrome 716708005
SNOMED CT code
| SNOMED code | 716708005 |
|---|---|
| name | FRAXF syndrome |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | FRAXF syndrome (disorder) |
| synonyms | FRAXF syndrome |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Chromosomal morphology 107675007 |
| Occurrence | Congenital 255399007 |
| Finding site | Sex chromosome X 72837006 |
| parents | |
| 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 FRAXF syndrome 716708005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 FRAXF syndrome 716708005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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