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 |
| 115650017 | Adenosylcobalamin synthesis defect | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 115651018 | Adenosylcobalamin synthesis defect, NOS | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 115652013 | Methylmalonic aciduria, type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 809579010 | Adenosylcobalamin synthesis defect (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1216875018 | Methylmalonic acidaemia due to defects in adenosylcobalamin biosynthesis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1216876017 | Methylmalonic acidaemia due to defects in adenosylcobalamin biosynthesis (disorder) | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 1216877014 | Vitamin B12-responsive methylmalonic acidaemia | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1218362019 | Methylmalonic acidemia due to defects in adenosylcobalamin biosynthesis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1218363012 | Vitamin B12-responsive methylmalonic acidemia | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1218364018 | Methylmalonic acidemia due to defects in adenosylcobalamin biosynthesis (disorder) | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Adenosylcobalamin synthesis defect | Is a | Methylmalonic acidemia | true | Inferred relationship | Existential restriction modifier | ||
| Adenosylcobalamin synthesis defect | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Adenosylcobalamin synthesis defect | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cobalamin A disease | Is a | True | Adenosylcobalamin synthesis defect | Inferred relationship | Existential restriction modifier | |
| Cobalamin B disease | Is a | True | Adenosylcobalamin synthesis defect | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR