Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4964346017 | Autosomal recessive congenital fiber-type disproportion myopathy due to TPM3 mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4964347014 | Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4964348016 | Autosomal recessive congenital fibre-type disproportion myopathy due to tropomyosin 3 mutation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4964349012 | Autosomal recessive congenital fibre-type disproportion myopathy due to TPM3 mutation | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4964350012 | Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation | Is a | Congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation | Associated morphology | Morphologically abnormal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive congenital fiber-type disproportion myopathy due to tropomyosin 3 mutation | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR