Bone dysplasia lethal Holmgren type 732249002
SNOMED CT code
| SNOMED code | 732249002 |
|---|---|
| name | Bone dysplasia lethal Holmgren type |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Bone dysplasia lethal Holmgren type (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dysplasia 25723000 |
| Finding site | Bone structure of extremity 48566001 |
| attributes - group2 | |
| Interprets | Limb length 164835000 |
| Has interpretation | Below reference range 281300000 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Rhizomelic dysplasia 1263463009 Bone dysplasia lethal Holmgren type 732249002 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 Bone dysplasia lethal Holmgren type 732249002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Bone dysplasia lethal Holmgren type 732249002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Bone dysplasia lethal Holmgren type 732249002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Bone dysplasia lethal Holmgren type 732249002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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