Smith McCort dysplasia 715862006
SNOMED CT code
SNOMED code | 715862006 |
---|---|
name | Smith McCort dysplasia |
status | active |
date introduced | 2016-07-31 |
fully specified name(s) | Smith McCort dysplasia (disorder) |
synonyms | Smith McCort dysplasia |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dysplasia 25723000 |
Finding site | Bone structure of extremity 48566001 |
attributes - group3 | |
Interprets | Limb length 164835000 |
Has interpretation | Below reference range 281300000 |
attributes - group2 | |
Interprets | Body height measure 50373000 |
Has interpretation | Below reference range 281300000 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Rhizomelic dysplasia 1263463009 Smith McCort dysplasia 715862006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Metaphyseal chondrodysplasia 28681006 Spondyloepimetaphyseal disorder 254062008 Smith McCort dysplasia 715862006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Smith McCort dysplasia 715862006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Smith McCort dysplasia 715862006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Smith McCort dysplasia 715862006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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