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FHIR Server FHIR Server 3.7.22-SNAPSHOT
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FHIR Version n/a
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FHIR
© HL7.org
|
Server Home |
FHIR Server FHIR Server 3.7.22-SNAPSHOT
|
FHIR Version n/a
User: [n/a]
Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2015. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5449908013 | A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5449909017 | A rare syndrome characterized by hypokalemic metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3031308017 | Gitelman's syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3031375018 | Gitelman syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3031384018 | Gitelman syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Hypocalciuria | false | Inferred relationship | Some | ||
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Familial hypokalemic and hypomagnesemic tubulopathy | false | Inferred relationship | Some | ||
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Associated morphology | Inflammation | false | Inferred relationship | Some | 2 | |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Finding site | Structure of parenchyma of kidney | false | Inferred relationship | Some | 2 | |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Associated morphology | Inflammation | false | Inferred relationship | Some | 3 | |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Finding site | Structure of interstitial tissue of kidney | false | Inferred relationship | Some | 3 | |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Renal hypocalciuria (disorder) | true | Inferred relationship | Some | ||
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Finding site | Structure of interstitial tissue of kidney | true | Inferred relationship | Some | 1 | |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Finding site | Renal tubule structure | true | Inferred relationship | Some | 2 | |
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Connective tissue hereditary disorder | true | Inferred relationship | Some | ||
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Hypokalemic alkalosis | true | Inferred relationship | Some | ||
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Hypokalemic nephropathy | true | Inferred relationship | Some | ||
| A rare syndrome characterised by hypokalaemic metabolic alkalosis in combination with significant hypomagnesaemia and low urinary calcium excretion. | Is a | Primary hypomagnesemia | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)