7p22.1 microduplication syndrome 764703002
SNOMED CT code
| SNOMED code | 764703002 |
|---|---|
| name | 7p22.1 microduplication syndrome |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | 7p22.1 microduplication syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Short arm of chromosome 278145009 |
| Associated morphology | Partial trisomy 133849008 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Chromosome pair 7 70488008 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Partial trisomy 133849008 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 7p22.1 microduplication syndrome 764703002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 7p22.1 microduplication syndrome 764703002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chromosomal disorder 409709004 Congenital chromosomal disease 74345006 Trisomy and partial trisomy of autosome 270521004 Trisomy 7 205648000 Partial trisomy of chromosome 7 726346004 7p partial trisomy 82751009 7p22.1 microduplication syndrome 764703002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 7p22.1 microduplication syndrome 764703002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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