1p36 deletion syndrome 699306003
SNOMED CT code
| SNOMED code | 699306003 |
|---|---|
| name | 1p36 deletion syndrome |
| status | active |
| date introduced | 2014-01-31 |
| fully specified name(s) | Chromosome 1p36 deletion syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Short arm of chromosome 278145009 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Partial monosomy 371169004 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Partial monosomy 371169004 |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 1 46507000 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 1p36 deletion syndrome 699306003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Anomaly of chromosome pair 362984008 Anomaly of chromosome pair 1 74769007 Deletion of part of chromosome 1 726365007 1p partial monosomy 36369001 1p36 deletion syndrome 699306003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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