Achondrogenesis, type IB 14870002
SNOMED CT code
| SNOMED code | 14870002 |
|---|---|
| name | Achondrogenesis, type IB |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Achondrogenesis, type IB (disorder) |
| synonyms | Achondrogenesis, type IB |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Hypoplasia 55199003 |
| Finding site | Bone structure 272673000 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skeletal system structure 113192009 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group3 | |
| Interprets | Height / growth measure 271603002 |
| 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 Achondrogenesis 2391001 Achondrogenesis, type IB 14870002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Achondrogenesis, type IB 14870002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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