Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3763716019 | Autosomal recessive spastic ataxia type 4 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3763717011 | Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3763718018 | Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3763719014 | SPAX 4 - autosomal recessive spastic ataxia type 4 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Hereditary disorder of the visual system | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Hereditary ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Finding site | Optic nerve structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Associated morphology | Atrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Optic atrophy | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Cerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Second cranial nerve finding | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Dysarthria | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Mitochondrial cytopathy | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Inherited optic neuropathy | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR