Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-May 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5045361018 | Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 5045362013 | RARS-related autosomal recessive hypomyelinating leucodystrophy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 5045363015 | Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 5045364014 | RARS-related autosomal recessive hypomyelinating leukodystrophy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 5045365010 | Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leucodystrophy | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Is a | Intellectual disability | true | Inferred relationship | Existential restriction modifier | ||
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Is a | Leukodystrophy | true | Inferred relationship | Existential restriction modifier | ||
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 3 | |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Finding site | Myelinated nerve fiber structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Associated morphology | Myelin sheath alteration | true | Inferred relationship | Existential restriction modifier | 1 | |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Finding site | White matter structure of brain and spinal cord | true | Inferred relationship | Existential restriction modifier | 2 | |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 2 | |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Interprets | Adaptation behavior | true | Inferred relationship | Existential restriction modifier | 4 | |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 4 | |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Interprets | Intellectual ability | true | Inferred relationship | Existential restriction modifier | 5 | |
| Arginyl-tRNA synthetase 1-related autosomal recessive hypomyelinating leukodystrophy | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 5 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR