Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
59927015 | Aminoaciduria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
767605014 | Aminoaciduria (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Aminoaciduria | Is a | Disorder of amino acid metabolism | true | Inferred relationship | Existential restriction modifier | ||
Aminoaciduria | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
Aminoaciduria | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Lysinuric protein intolerance | Is a | False | Aminoaciduria | Inferred relationship | Existential restriction modifier | |
Imidazole aminoaciduria | Is a | True | Aminoaciduria | Inferred relationship | Existential restriction modifier | |
Benign neonatal hyperaminoaciduria | Is a | False | Aminoaciduria | Inferred relationship | Existential restriction modifier | |
Inherited aminoaciduria | Is a | True | Aminoaciduria | Inferred relationship | Existential restriction modifier | |
Deficiency of aminoacylase 1 | Has definitional manifestation | False | Aminoaciduria | Inferred relationship | Existential restriction modifier | |
Inherited aminoaciduria | Is a | False | Aminoaciduria | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets