Campomelia Cumming type 720599002
SNOMED CT code
| SNOMED code | 720599002 | ||
|---|---|---|---|
| name | Campomelia Cumming type | ||
| status | active | ||
| date introduced | 2017-01-31 | ||
| fully specified name(s) | Campomelia Cumming type (disorder) | ||
| synonyms |
| ||
| attributes - group2 | |||
| Pathological process | Pathological developmental process 308490002 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Bone structure of extremity 48566001 | ||
| Associated morphology | Congenital abnormal curvature 38392006 | ||
| attributes - group1 | |||
| Pathological process | Pathological developmental process 308490002 | ||
| Occurrence | Congenital 255399007 | ||
| Finding site | Bone structure 272673000 | ||
| Associated morphology | Dysplasia 25723000 | ||
| attributes - group3 | |||
| Associated morphology | Lymphatic edema 30213001 | ||
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Edema 267038008 Disorder characterized by edema 118654009 Lymphedema 234097001 Hereditary lymphedema 254199006 Campomelia Cumming type 720599002 SNOMED CT Concept 138875005 Clinical finding 404684003 Deformity 417893002 Deformity of bone 271084006 Campomelia Cumming type 720599002 SNOMED CT Concept 138875005 Clinical finding 404684003 Deformity 417893002 Congenital deformity 276655000 Campomelia Cumming type 720599002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Bent bone dysplasia group 278832007 Campomelia Cumming type 720599002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Campomelia Cumming type 720599002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with limb defect as major feature 41443008 Campomelia Cumming type 720599002 SNOMED CT Concept 138875005 Clinical finding 404684003 Deformity 417893002 Deformity of limb 445144002 Campomelia Cumming type 720599002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of extremity 128605003 Congenital anomaly of limb 60475009 Campomelia Cumming type 720599002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Campomelia Cumming type 720599002 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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