Spondyloepimetaphyseal dysplasia, Strudwick type 702350003
SNOMED CT code
| SNOMED code | 702350003 |
|---|---|
| name | Spondyloepimetaphyseal dysplasia, Strudwick type |
| status | active |
| date introduced | 2014-07-31 |
| fully specified name(s) | Spondyloepimetaphyseal dysplasia, Strudwick type (disorder) |
| synonyms |
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| attributes - group1 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Osteochondrodysplasia syndrome 105985007 Spondyloepimetaphyseal dysplasia, Strudwick type 702350003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Spondyloepimetaphyseal dysplasia, Strudwick type 702350003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Spondyloepimetaphyseal dysplasia, Strudwick type 702350003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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