Fibrochondrogenesis 17144009
SNOMED CT code
| SNOMED code | 17144009 |
|---|---|
| name | Fibrochondrogenesis |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Fibrochondrogenesis (disorder) |
| synonyms | Fibrochondrogenesis |
| attributes - group1 | |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure 272673000 |
| 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 Fibrochondrogenesis 17144009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Chondrodysplasia 205465004 Fibrochondrogenesis 17144009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Fibrochondrogenesis 17144009 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Fibrochondrogenesis 17144009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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