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1197059004: Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder)


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


0 descendants.

Expanded Value Set


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

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