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 |
| 356726016 | CPTII - Carnitine palmitoyltransferase deficiency type II | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 356727013 | Muscle form of carnitine palmitoyltransferase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 356728015 | CPT2 - Carnitine palmitoyltransferase II deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 356729011 | Carnitine palmitoyltransferase II deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 626818013 | Carnitine palmitoyltransferase II deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3036673017 | Carnitine palmitoyltransferase deficiency type 2 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Carnitine palmitoyltransferase II deficiency | Is a | Carnitine palmitoyltransferase deficiency | true | Inferred relationship | Existential restriction modifier | ||
| Carnitine palmitoyltransferase II deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Carnitine palmitoyltransferase II deficiency | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Carnitine palmitoyltransferase II deficiency | Is a | Fatty acid oxidation defect | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Severe infantile form of carnitine palmitoyltransferase II deficiency | Is a | True | Carnitine palmitoyltransferase II deficiency | Inferred relationship | Existential restriction modifier | |
| Neonatal form of carnitine palmitoyltransferase II deficiency | Is a | True | Carnitine palmitoyltransferase II deficiency | Inferred relationship | Existential restriction modifier | |
| Myopathic form of carnitine palmitoyltransferase II deficiency | Is a | True | Carnitine palmitoyltransferase II deficiency | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR