Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4694784017 | Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
4694785016 | Congenital ichthyosis, microcephalus, tetraplegia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
4694786015 | Congenital ichthyosis, microcephalus, quadriplegia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
4694787012 | A rare autosomal ichthyosis syndrome with prominent neurologic signs and the association of congenital ichthyosis with severe developmental delay, microcephaly, spastic tetraplegia, sensorineural hearing impairment, athetosis, and myoclonus. Marked epileptic discharges with occurrence of tonic spasms have also been reported. Cerebral MRI shows diffuse cortical atrophy. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Decreased hearing | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Microcephaly | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Myopathy | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Congenital ichthyosis of skin | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Myoclonus | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Spastic tetraplegia | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Developmental delay | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Auditory system hereditary disorder | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Athetosis | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Is a | Sensorineural hearing loss | true | Inferred relationship | Some | ||
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Interprets | Movement | true | Inferred relationship | Some | 9 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Finding site | Limb structure | true | Inferred relationship | Some | 5 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Finding site | Muscle structure | true | Inferred relationship | Some | 6 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Finding site | Extrapyramidal system structure | true | Inferred relationship | Some | 7 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Finding site | Structure of auditory system | true | Inferred relationship | Some | 8 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Interprets | Hearing | true | Inferred relationship | Some | 2 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Has interpretation | Decreased | true | Inferred relationship | Some | 2 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Interprets | Keratinisation | true | Inferred relationship | Some | 3 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Has interpretation | Abnormal | true | Inferred relationship | Some | 3 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Interprets | Head circumference | true | Inferred relationship | Some | 4 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Has interpretation | Below reference range | true | Inferred relationship | Some | 4 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Finding site | Entire skin | true | Inferred relationship | Some | 1 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 1 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Interprets | Movement observable | true | Inferred relationship | Some | 10 | |
Congenital ichthyosis, microcephalus, tetraplegia syndrome | Has interpretation | Absent | true | Inferred relationship | Some | 10 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
REPLACED BY association reference set