Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Nov 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4667503012 | Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 4667504018 | Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | Intellectual disability | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | Complicated hereditary spastic paraplegia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | Disorder of lipid metabolism | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Finding site | Spinal cord structure | false | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Associated morphology | Degenerative abnormality | false | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 3 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Finding site | Lower limb structure | false | Inferred relationship | Existential restriction modifier | 3 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | Autosomal recessive hereditary spastic paraplegia | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | Chronic metabolic disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Is a | Chronic mental disorder | false | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 4 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Finding site | Lower limb structure | false | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Finding site | Spinal cord structure | true | Inferred relationship | Existential restriction modifier | 3 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Associated morphology | Degenerative abnormality | true | Inferred relationship | Existential restriction modifier | 3 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Interprets | Intellectual ability | true | Inferred relationship | Existential restriction modifier | 5 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 5 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Interprets | Adaptation behavior | true | Inferred relationship | Existential restriction modifier | 6 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Has interpretation | Impaired | true | Inferred relationship | Existential restriction modifier | 6 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Interprets | Movement | true | Inferred relationship | Existential restriction modifier | 7 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Finding site | Structure of right lower limb | true | Inferred relationship | Existential restriction modifier | 2 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Finding site | Structure of left lower limb | true | Inferred relationship | Existential restriction modifier | 8 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Has interpretation | Absent | true | Inferred relationship | Existential restriction modifier | 9 | |
| Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction | Interprets | Movement observable | true | Inferred relationship | Existential restriction modifier | 9 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR