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 |
| 134168018 | Inherited methylmalonic acidemia AND homocystinuria | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 134169014 | Inherited methylmalonic acidemia and homocystinuria | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 504532010 | CblF - Cobalamin locus F variant | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 504533017 | Cobalamin locus F variant | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 504534011 | CblF methylmalonic acidemia and homocystinuria | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 504535012 | Inherited methylmalonic acidaemia AND homocystinuria | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 504536013 | CblF methylmalonic acidaemia and homocystinuria | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 822096011 | Inherited methylmalonic acidemia AND homocystinuria (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited methylmalonic acidemia AND homocystinuria | Is a | Adenosylcobalamin and methylcobalamin synthesis defect | true | Inferred relationship | Existential restriction modifier | ||
| Inherited methylmalonic acidemia AND homocystinuria | Is a | Homocystinuria | true | Inferred relationship | Existential restriction modifier | ||
| Inherited methylmalonic acidemia AND homocystinuria | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Inherited methylmalonic acidemia AND homocystinuria | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Inherited methylmalonic acidemia AND homocystinuria | Is a | Hereditary disease | false | Inferred relationship | Existential restriction modifier | ||
| Inherited methylmalonic acidemia AND homocystinuria | Is a | Hereditary metabolic disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR