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 |
| 7715018 | Adenosylcobalamin and methylcobalamin synthesis defect | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 7716017 | Adenosylcobalamin and methylcobalamin synthesis defect, NOS | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 493787010 | Combined methylmalonic acidaemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 493788017 | Combined methylmalonic acidemia and homocystinuria due to defects in adenosylcobalamin and methylcobalamin synthesis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 781178011 | Adenosylcobalamin and methylcobalamin synthesis defect (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Adenosylcobalamin and methylcobalamin synthesis defect | Is a | Methylmalonic acidemia | true | Inferred relationship | Existential restriction modifier | ||
| Adenosylcobalamin and methylcobalamin synthesis defect | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Adenosylcobalamin and methylcobalamin synthesis defect | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cobalamin D disease | Is a | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Existential restriction modifier | |
| Cobalamin A disease | Is a | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Existential restriction modifier | |
| Cobalamin C disease | Is a | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Existential restriction modifier | |
| Inherited methylmalonic acidemia AND homocystinuria | Is a | True | Adenosylcobalamin and methylcobalamin synthesis defect | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR