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 |
| 476093013 | Holocarboxylase synthase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 740045012 | Holocarboxylase synthase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3957559014 | Neonatal multiple carboxylase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3957560016 | Early-onset multiple carboxylase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Holocarboxylase synthase deficiency | Is a | Disorder of branched-chain amino acid metabolism | false | Inferred relationship | Existential restriction modifier | ||
| Holocarboxylase synthase deficiency | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Holocarboxylase synthase deficiency | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Holocarboxylase synthase deficiency | Is a | Biotinidase deficiency | false | Inferred relationship | Existential restriction modifier | ||
| Holocarboxylase synthase deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Holocarboxylase synthase deficiency | Is a | Multiple carboxylase deficiency | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR