Diastrophic dysplasia 58561002
SNOMED CT code
| SNOMED code | 58561002 |
|---|---|
| name | Diastrophic dysplasia |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Diastrophic dysplasia (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Bone structure 272673000 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Congenital smallness 41086002 |
| Finding site | Entire limb 243996003 |
| Occurrence | Congenital 255399007 |
| attributes - group4 | |
| Interprets | Range of joint movement 364564000 |
| Has interpretation | Decreased 1250004 |
| attributes - group5 | |
| Interprets | Body height measure 50373000 |
| Has interpretation | Below reference range 281300000 |
| attributes - group3 | |
| Finding site | Structure of joint region 785818007 |
| Associated morphology | Contracture 57048009 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Disorder of skeletal system 88230002 Skeletal dysplasia 105986008 Diastrophic dysplasia 58561002 SNOMED CT Concept 138875005 Clinical finding 404684003 Deformity 417893002 Contracture of joint 7890003 Contracture of multiple joints 202264009 Diastrophic dysplasia 58561002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Diastrophic dysplasia 58561002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Diastrophic dysplasia 58561002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Diastrophic dysplasia 58561002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Micromelia 74370006 Diastrophic dysplasia 58561002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Diastrophic dysplasia 58561002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Diastrophic dysplasia 58561002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Diastrophic dysplasia 58561002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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