Hypochondroplasia 205468002
SNOMED CT code
| SNOMED code | 205468002 |
|---|---|
| name | Hypochondroplasia |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hypochondroplasia (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| Finding site | Bone structure 272673000 |
| attributes - group2 | |
| 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 Hypochondroplasia 205468002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Congenital malformation syndromes associated with short stature 205808005 Hypochondroplasia 205468002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Hypochondroplasia 205468002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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