Trisomy 13, meiotic nondisjunction 205619006
SNOMED CT code
| SNOMED code | 205619006 |
|---|---|
| name | Trisomy 13, meiotic nondisjunction |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Trisomy 13, meiotic nondisjunction (disorder) |
| synonyms | Trisomy 13, meiotic nondisjunction |
| attributes - group1 | |
| Associated morphology | Trisomy 78989007 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 13 55401003 |
| 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 Complete trisomy 13 syndrome 21111006 Trisomy 13, meiotic nondisjunction 205619006 SNOMED CT Concept 138875005 Clinical 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 13, meiotic nondisjunction 205619006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Trisomy 13, meiotic nondisjunction 205619006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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