Brachyolmia 254088006
SNOMED CT code
| SNOMED code | 254088006 |
|---|---|
| name | Brachyolmia |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Brachyolmia (disorder) |
| synonyms | Brachyolmia |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| Finding site | Bone structure 272673000 |
| attributes - group2 | |
| Interprets | Height / growth measure 271603002 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Brachyolmia 254088006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Congenital malformation syndromes associated with short stature 205808005 Brachyolmia 254088006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Spondylodysplastic group 278708009 Brachyolmia 254088006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Brachyolmia 254088006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Brachyolmia 254088006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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