Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
91537011 | Hepatic porphyria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
793355018 | Hepatic porphyria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hepatic porphyria | Is a | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
Hepatic porphyria | Is a | Digestive system hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Hepatic porphyria | Is a | Disease of liver | true | Inferred relationship | Some | ||
Hepatic porphyria | Is a | Congenital anomaly of digestive system | false | Inferred relationship | Some | ||
Hepatic porphyria | Is a | Porphyria | false | Inferred relationship | Some | ||
Hepatic porphyria | Finding site | Liver structure | true | Inferred relationship | Some | 1 | |
Hepatic porphyria | Occurrence | Congenital | false | Inferred relationship | Some | ||
Hepatic porphyria | Is a | Disorder of porphyrin metabolism | false | Inferred relationship | Some | ||
Hepatic porphyria | Is a | Porphyria (disorder) | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Variegate porphyria | Is a | True | Hepatic porphyria | Inferred relationship | Some | |
Porphyria cutanea tarda | Is a | True | Hepatic porphyria | Inferred relationship | Some | |
Benign recurrent intrahepatic cholestasis | Is a | False | Hepatic porphyria | Inferred relationship | Some | |
Rotor syndrome | Is a | False | Hepatic porphyria | Inferred relationship | Some | |
Dubin-Johnson syndrome | Is a | False | Hepatic porphyria | Inferred relationship | Some | |
Familial arthrogryposis-cholestatic hepatorenal syndrome | Is a | False | Hepatic porphyria | Inferred relationship | Some | |
Progressive intrahepatic cholestasis | Is a | False | Hepatic porphyria | Inferred relationship | Some | |
Crigler-Najjar syndrome, type I | Is a | False | Hepatic porphyria | Inferred relationship | Some | |
Hereditary coproporphyria | Is a | True | Hepatic porphyria | Inferred relationship | Some |
This concept is not in any reference sets