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 |
| 104006016 | Congenital defect of folate absorption | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 104007013 | Congenital malabsorption of folic acid | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 104008015 | Folic acid transport defect | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 801765019 | Congenital defect of folate absorption (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1232350015 | Hereditary folate malabsorption | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1232351016 | Folate transport defect | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital defect of folate absorption | Is a | Inherited disorder of folate metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Congenital defect of folate absorption | Is a | Disorder of sulfur-bearing amino acid metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Congenital defect of folate absorption | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital defect of folate absorption | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR