Achondrogenesis, type II 254061001
SNOMED CT code
SNOMED code | 254061001 |
---|---|
name | Achondrogenesis, type II |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Achondrogenesis, type II (disorder) |
synonyms |
|
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 |
Occurrence | Congenital 255399007 |
Associated morphology | Dysplasia 25723000 |
Finding site | Bone structure 272673000 |
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 II 254061001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Spondyloepiphyseal dysplasia congenita 278713008 Achondrogenesis, type II 254061001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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