Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3763840015 | Beta-mercaptolactate cysteine disulfiduria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3763841016 | Ampola syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3763842011 | Beta-mercaptolactate cysteine disulfiduria | en | Synonym | Active | Case insensitive | SNOMED CT core |
3763843018 | An extremely rare disorder of methionine cycle and sulfur amino acid metabolism with characteristics of increased urine excretion of beta-mercaptolactate-cysteine disulfide (due to deficiency of mercaptopyruvate sulfurtransferase activity in erythrocytes), leading to a positive cyanide nitroprusside test. Association with intellectual disability, congenital lens dislocation, and behavioral abnormalities has been reported, however the causal link remains to be established. There have been no further descriptions in the literature since 1981. | en | Definition | Active | Case sensitive | SNOMED CT core |
3763844012 | An extremely rare disorder of methionine cycle and sulphur amino acid metabolism with characteristics of increased urine excretion of beta-mercaptolactate-cysteine disulfide (due to deficiency of mercaptopyruvate sulfurtransferase activity in erythrocytes), leading to a positive cyanide nitroprusside test. Association with intellectual disability, congenital lens dislocation, and behavioural abnormalities has been reported, however the causal link remains to be established. There have been no further descriptions in the literature since 1981. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Beta-mercaptolactate cysteine disulfiduria | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Beta-mercaptolactate cysteine disulfiduria | Is a | Disorder of sulfur-bearing amino acid metabolism | true | Inferred relationship | Some | ||
Beta-mercaptolactate cysteine disulfiduria | Due to | Deficiency of 3-mercaptopyruvate sulfurtransferase | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set