Brachydactyly type B2 770406002
SNOMED CT code
| SNOMED code | 770406002 |
|---|---|
| name | Brachydactyly type B2 |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Brachydactyly type B2 (disorder) |
| synonyms | Brachydactyly type B2 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Ankylosis 36504009 |
| Occurrence | Congenital 255399007 |
| Finding site | Interphalangeal joint structure 416599001 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Digit structure 82680008 |
| Associated morphology | Abnormally short growth 11182007 |
| Occurrence | Congenital 255399007 |
| 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 Brachydactyly type B2 770406002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Disorder of digit 128597007 Congenital anomaly of digit 403855001 Symphalangism 253975004 Brachydactyly type B2 770406002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Brachydactyly type B2 770406002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Brachydactyly type B2 770406002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Deformity of limb 445144002 Longitudinal deficiency of part of limb 716638009 Brachydactyly 43476002 Brachydactyly type B2 770406002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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