Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
102819015 | Porphyria cutanea tarda | en | Synonym | Active | Case insensitive | SNOMED CT core |
102821013 | Symptomatic porphyria | en | Synonym | Active | Case insensitive | SNOMED CT core |
102822018 | Cutaneous hepatic porphyria | en | Synonym | Active | Case insensitive | SNOMED CT core |
102823011 | PCT | en | Synonym | Active | Case sensitive | SNOMED CT core |
102824017 | Porphyria cutanea tarda symptomatica | en | Synonym | Active | Case insensitive | SNOMED CT core |
102825016 | Porphyria, hepatocutaneous type | en | Synonym | Active | Case insensitive | SNOMED CT core |
102826015 | Urocoproporphyria | en | Synonym | Active | Case insensitive | SNOMED CT core |
102827012 | UROD deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
499144011 | PCT - Porphyria cutanea tarda | en | Synonym | Active | Case sensitive | SNOMED CT core |
499145012 | CHP - Cutaneous hepatic porphyria | en | Synonym | Active | Case sensitive | SNOMED CT core |
800968016 | Porphyria cutanea tarda (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Porphyria cutanea tarda | Is a | Disorder of skin | true | Inferred relationship | Some | ||
Porphyria cutanea tarda | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Porphyria cutanea tarda | Is a | Congenital anomaly of integument | false | Inferred relationship | Some | ||
Porphyria cutanea tarda | Is a | Hepatic porphyria | true | Inferred relationship | Some | ||
Porphyria cutanea tarda | Is a | Uroporphyrinogen decarboxylase deficiency | true | Inferred relationship | Some | ||
Porphyria cutanea tarda | Is a | Disorder of soft tissue of body cavity | false | Inferred relationship | Some | ||
Porphyria cutanea tarda | Is a | Disorder of soft tissue of body cavity | false | Inferred relationship | Some | ||
Porphyria cutanea tarda | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
Porphyria cutanea tarda | Occurrence | Congenital | false | Inferred relationship | Some | ||
Porphyria cutanea tarda | Finding site | Liver structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Acquired porphyria cutanea tarda | Is a | True | Porphyria cutanea tarda | Inferred relationship | Some | |
Sporadic porphyria cutanea tarda | Is a | True | Porphyria cutanea tarda | Inferred relationship | Some | |
Familial porphyria cutanea tarda | Is a | True | Porphyria cutanea tarda | Inferred relationship | Some | |
Neonatal jaundice with porphyria | Associated with | False | Porphyria cutanea tarda | Inferred relationship | Some | |
Homozygous porphyria cutanea tarda | Is a | True | Porphyria cutanea tarda | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set