Leri-Weill dyschondrosteosis 17818006
SNOMED CT code
| SNOMED code | 17818006 |
|---|---|
| name | Leri-Weill dyschondrosteosis |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Leri-Weill dyschondrosteosis (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure of left radius 719464007 |
| attributes - group3 | |
| Interprets | Limb length 164835000 |
| Has interpretation | Below reference range 281300000 |
| attributes - group2 | |
| Finding site | Bone structure of right radius 719465008 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure of distal right ulna 719612005 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group5 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of right radiocarpal joint 720555006 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group6 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of left radiocarpal joint 720556007 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group7 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure of distal left ulna 719611003 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group8 | |
| Interprets | Body height 1153637007 |
| Has interpretation | Below reference range 281300000 |
| 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 Autosomal dominant hereditary disorder 11164009 Leri-Weill dyschondrosteosis 17818006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Mesomelic dysplasia 205473008 Leri-Weill dyschondrosteosis 17818006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Leri-Weill dyschondrosteosis 17818006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Leri-Weill dyschondrosteosis 17818006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Leri-Weill dyschondrosteosis 17818006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Finding of upper limb 116307009 Finding of bone of upper limb 298756009 Lesion of bone of left radius and/or ulna 16302391000119104 Bilateral Madelung deformity 890380004 Leri-Weill dyschondrosteosis 17818006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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