FHIR
© HL7.org
|
Server Home |
FHIR Server FHIR Server 3.7.22-SNAPSHOT
|
FHIR Version n/a
User: [n/a]
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 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 7715018 | Adenosylcobalamin and methylcobalamin synthesis defect | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 493787010 | Combined methylmalonic acidaemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 493788017 | Combined methylmalonic acidemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 781178011 | Adenosylcobalamin and methylcobalamin synthesis defect (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5938661000241111 | défaut de synthèse de l'adénosylcobalamine et de la methylcobalamine | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 5938681000241118 | synthèse défectueuse de l'adénosylcobalamine et de la méthylcobalamine | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Adenosylcobalamin and methylcobalamin synthesis defect | Is a | Methylmalonic acidemia | true | Inferred relationship | Some | ||
| Adenosylcobalamin and methylcobalamin synthesis defect | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Adenosylcobalamin and methylcobalamin synthesis defect | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cobalamin D disease (disorder) | Is a | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Some | |
| Cobalamin A disease | Is a | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Some | |
| Cobalamin C disease | Is a | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Some | |
| Inherited methylmalonic acidemia AND homocystinuria | Is a | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Some |
This concept is not in any reference sets