Chromosome Xq27.3q28 duplication syndrome 718881004
SNOMED CT code
| SNOMED code | 718881004 |
|---|---|
| name | Chromosome Xq27.3q28 duplication syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Chromosome Xq27.3q28 duplication syndrome (disorder) |
| synonyms | Chromosome Xq27.3q28 duplication syndrome |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Sex chromosome X 72837006 |
| Associated morphology | Partial trisomy 133849008 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Long arm of chromosome 312242007 |
| Associated morphology | Partial trisomy 133849008 |
| Occurrence | Congenital 255399007 |
| 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 Chromosome Xq27.3q28 duplication syndrome 718881004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 Chromosome Xq27.3q28 duplication syndrome 718881004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Chromosome Xq27.3q28 duplication syndrome 718881004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Chromosome Xq27.3q28 duplication syndrome 718881004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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