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 |
| 49668019 | Combined molybdoflavoprotein enzyme deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 49669010 | Hereditary xanthinuria, type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 49670011 | Deficiency of molybdenum cofactor | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 49671010 | Xanthine oxidase-sulfite oxidase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484364013 | Hereditary xanthinuria type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484365014 | Molybdenum cofactor deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484366010 | Combined xanthine oxidase and aldehyde oxidase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484367018 | Xanthine oxidase-sulphite oxidase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484368011 | Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 484369015 | Combined xanthine oxidase and sulphite oxidase and aldehyde oxidase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 760614019 | Combined molybdoflavoprotein enzyme deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Combined molybdoflavoprotein enzyme deficiency | Is a | Hereditary xanthinuria | true | Inferred relationship | Existential restriction modifier | ||
| Combined molybdoflavoprotein enzyme deficiency | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Combined molybdoflavoprotein enzyme deficiency | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Molybdenum cofactor deficiency complementation group C | Is a | True | Combined molybdoflavoprotein enzyme deficiency | Inferred relationship | Existential restriction modifier | |
| Molybdenum cofactor deficiency complementation group A | Is a | True | Combined molybdoflavoprotein enzyme deficiency | Inferred relationship | Existential restriction modifier | |
| Molybdenum cofactor deficiency complementation group B | Is a | True | Combined molybdoflavoprotein enzyme deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR