Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
16993011 | Hyperphosphatasemia with bone disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
16994017 | Chronic congenital idiopathic hyperphosphatasemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
16995016 | Familial idiopathic hyperphosphatasemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
16996015 | Familial osteoectasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
16997012 | Hyperostosis corticalis deformans juvenilis | en | Synonym | Active | Case insensitive | SNOMED CT core |
16998019 | Juvenile Paget disease | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
16999010 | Osteochalasia desmalis familiaris | en | Synonym | Active | Case insensitive | SNOMED CT core |
512746019 | Osteoectasia with hyperphosphatasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
512747011 | Chronic congenital idiopathic hyperphosphatasaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
512748018 | Hyperphosphatasaemia with bone disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
512749014 | Familial idiopathic hyperphosphatasaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
841761014 | Hyperphosphatasemia with bone disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Idiopathic hyperphosphatasaemia | Is a | False | Hyperphosphatasaemia with bone disease | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set