Spondylometaphyseal dysplasia Schmidt type 719304005
SNOMED CT code
| SNOMED code | 719304005 |
|---|---|
| name | Spondylometaphyseal dysplasia Schmidt type |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Spondylometaphyseal dysplasia Schmidt type (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Bone structure 272673000 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Spondylometaphyseal dysplasia Schmidt type 719304005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Spondylometaphyseal dysplasia 784006008 Spondylometaphyseal dysplasia Schmidt type 719304005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Spondylometaphyseal dysplasia Schmidt type 719304005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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