Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4675715014 | Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
4675716010 | Autosomal recessive spinocerebellar ataxia type 21 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
4675717018 | Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Is a | Spinocerebellar ataxia | true | Inferred relationship | Existential restriction modifier | ||
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Is a | Acute hepatic failure | true | Inferred relationship | Existential restriction modifier | ||
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Is a | Digestive system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Is a | Hereditary peripheral neuropathy | true | Inferred relationship | Existential restriction modifier | ||
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Finding site | Peripheral nervous system structure | true | Inferred relationship | Existential restriction modifier | 4 | |
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Occurrence | Infancy | true | Inferred relationship | Existential restriction modifier | 3 | |
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Finding site | Structure of parenchyma of liver | true | Inferred relationship | Existential restriction modifier | 3 | |
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Finding site | Cerebellar structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Existential restriction modifier | 1 | |
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Finding site | Spinal cord structure | true | Inferred relationship | Existential restriction modifier | 2 | |
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome | Associated morphology | Degenerative abnormality | true | Inferred relationship | Existential restriction modifier | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets