Camptodactyly syndrome Guadalajara type 2 720603002
SNOMED CT code
| SNOMED code | 720603002 |
|---|---|
| name | Camptodactyly syndrome Guadalajara type 2 |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Camptodactyly syndrome Guadalajara type 2 (disorder) |
| synonyms | Camptodactyly syndrome Guadalajara type 2 |
| attributes - group2 | |
| Finding site | Bone structure 272673000 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Fixed flexion deformity 788600005 |
| Finding site | Musculoskeletal structure of finger 310794003 |
| parents |
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| 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 Camptodactyly syndrome Guadalajara type 2 720603002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Finding of musculoskeletal structure of digit of hand 299055007 Finding of musculoskeletal structure of finger 299056008 Camptodactyly of finger 1162716000 Camptodactyly syndrome Guadalajara type 2 720603002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Camptodactyly syndrome Guadalajara type 2 720603002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Camptodactyly syndrome Guadalajara type 2 720603002 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 Camptodactyly syndrome Guadalajara type 2 720603002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Camptodactyly syndrome Guadalajara type 2 720603002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Camptodactyly syndrome Guadalajara type 2 720603002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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