XY, female phenotype 205693008
SNOMED CT code
| SNOMED code | 205693008 |
|---|---|
| name | XY, female phenotype |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | XY, female phenotype (disorder) |
| synonyms | XY, female phenotype |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Cellular AND/OR subcellular abnormality 107673000 |
| Finding site | Sex chromosome 32247007 |
| parents | Sex chromosome abnormality - female phenotype 254277006 |
| 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 Sex chromosome abnormality - female phenotype 254277006 XY, female phenotype 205693008 |
| ancestors | sorted most to least specific |
| cpt crosswalks | |
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