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2667000: Absent (qualifier value)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5527017 Absent en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5528010 Absence of en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
757146018 Absent (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Absent Is a General adjectival modifier false Inferred relationship Some
Absent Is a Absence findings true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder) Has interpretation True Absent Inferred relationship Some 4
Progressive supranuclear palsy Has interpretation True Absent Inferred relationship Some 4
Brachial plexus palsy due to birth trauma Has interpretation True Absent Inferred relationship Some 4
Spastic paralysis due to intracranial birth injury Has interpretation True Absent Inferred relationship Some 5
Phrenic nerve paralysis as birth trauma Has interpretation True Absent Inferred relationship Some 4
Spastic paralysis due to birth injury Has interpretation True Absent Inferred relationship Some 5
Spastic paralysis due to spinal birth injury Has interpretation True Absent Inferred relationship Some 5
Klumpke-Déjerine paralysis as birth trauma Has interpretation True Absent Inferred relationship Some 4
Erb-Duchenne palsy as birth trauma Has interpretation True Absent Inferred relationship Some 5
Upward gaze deviation (disorder) Has interpretation True Absent Inferred relationship Some 4
Monoplegia of leg dominant side as sequela of cerebrovascular disease (disorder) Has interpretation True Absent Inferred relationship Some 5
Monoplegia of left dominant lower limb (disorder) Has interpretation True Absent Inferred relationship Some 4
Monoplegia of left nondominant lower limb (disorder) Has interpretation True Absent Inferred relationship Some 4
Monoplegia of right dominant lower limb (disorder) Has interpretation True Absent Inferred relationship Some 4
Monoplegia of right nondominant lower limb (disorder) Has interpretation True Absent Inferred relationship Some 4
Spastic hemiplegia of left dominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Spastic hemiplegia of left nondominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Spastic hemiplegia of right dominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Spastic hemiplegia of right nondominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Monoplegia of lower limb due to and following cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 6
Monoplegia of left nondominant upper limb due to and following cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 5
Monoplegia of right nondominant upper limb due to and following cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 5
Monoplegia of upper limb due to and following cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 6
Flaccid hemiplegia of left dominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Flaccid hemiplegia of left nondominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Flaccid hemiplegia of right dominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Flaccid hemiplegia of right nondominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Hemiplegia of left dominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Hemiplegia of left nondominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Hemiplegia of right dominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Hemiplegia of right nondominant side (disorder) Has interpretation True Absent Inferred relationship Some 3
Monoplegia of right upper limb (disorder) Has interpretation True Absent Inferred relationship Some 4
Monoplegia of left upper limb (disorder) Has interpretation True Absent Inferred relationship Some 4
Hemiplegia of nondominant side due to and following ischemic cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 4
Hemiplegia of dominant side due to and following ischemic cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 4
Monoplegia of upper limb due to and following ischemic cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 5
Hemiplegia of nondominant side due to and following embolic cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 4
Paraplegia due to and following cerebrovascular accident (disorder) Has interpretation True Absent Inferred relationship Some 3
Acute paralytic poliomyelitis, vaccine-associated Has interpretation True Absent Inferred relationship Some 4
Acute bulbar poliomyelitis caused by Human poliovirus 2 Has interpretation True Absent Inferred relationship Some 3
Acute bulbar poliomyelitis caused by Human poliovirus 1 Has interpretation True Absent Inferred relationship Some 3
Acute paralytic poliomyelitis caused by Human poliovirus 1 (disorder) Has interpretation True Absent Inferred relationship Some 3
Acute paralytic poliomyelitis caused by Human poliovirus 2 Has interpretation True Absent Inferred relationship Some 3
Acute paralytic poliomyelitis caused by Human poliovirus 3 (disorder) Has interpretation True Absent Inferred relationship Some 3
Congenital fibrosis of inferior rectus muscle (disorder) Has interpretation True Absent Inferred relationship Some 4
Severe intellectual disability and progressive spastic paraplegia Has interpretation True Absent Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 27 Has interpretation True Absent Inferred relationship Some 4
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 3 (disorder) Has interpretation True Absent Inferred relationship Some 2
Severe intellectual disability, progressive spastic diplegia syndrome (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 69 Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 71 Has interpretation True Absent Inferred relationship Some 2
Autosomal spastic paraplegia type 72 Has interpretation True Absent Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 60 Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 66 Has interpretation True Absent Inferred relationship Some 4
Inherited congenital spastic tetraplegia Has interpretation True Absent Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 14 Has interpretation True Absent Inferred relationship Some 4
Hereditary sensory and autonomic neuropathy due to TECPR2 mutation Has interpretation True Absent Inferred relationship Some 7
Autosomal dominant spastic paraplegia type 38 (disorder) Has interpretation True Absent Inferred relationship Some 2
X-linked spastic paraplegia type 16 (disorder) Has interpretation True Absent Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 13 (disorder) Has interpretation True Absent Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 56 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 24 Has interpretation True Absent Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 8 Has interpretation True Absent Inferred relationship Some 3
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder) Has interpretation True Absent Inferred relationship Some 6
Bilateral progressive external ophthalmoplegia Has interpretation True Absent Inferred relationship Some 5
Hemiparesis of left side of face (disorder) Has interpretation True Absent Inferred relationship Some 1
Hemiparesis of right side of face (disorder) Has interpretation True Absent Inferred relationship Some 1
Benedikt's syndrome Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant progressive external ophthalmoplegia type 5 Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant progressive external ophthalmoplegia type 3 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant progressive external ophthalmoplegia type 4 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant progressive external ophthalmoplegia type 1 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) Has interpretation True Absent Inferred relationship Some 4
Atypical progressive supranuclear palsy syndrome Has interpretation True Absent Inferred relationship Some 4
X-linked complex hereditary spastic paraplegia Has interpretation True Absent Inferred relationship Some 4
X-linked pure hereditary spastic paraplegia Has interpretation True Absent Inferred relationship Some 2
Progressive supranuclear palsy corticobasal syndrome (disorder) Has interpretation True Absent Inferred relationship Some 4
Progressive supranuclear palsy parkinsonism syndrome (disorder) Has interpretation True Absent Inferred relationship Some 5
Progressive supranuclear palsy progressive non fluent aphasia Has interpretation True Absent Inferred relationship Some 4
Exophthalmic ophthalmoplegia Has interpretation True Absent Inferred relationship Some 3
Monoparesis of lower limb Has interpretation True Absent Inferred relationship Some 3
Hemiplegia and/or hemiparesis following stroke Has interpretation True Absent Inferred relationship Some 4
Hemiparesis as late effect of cerebrovascular disease Has interpretation True Absent Inferred relationship Some 4
Monoplegia of arm dominant side as sequela of cerebrovascular disease Has interpretation True Absent Inferred relationship Some 5
Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome Has interpretation True Absent Inferred relationship Some 8
Autosomal recessive spastic paraplegia type 76 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 74 Has interpretation True Absent Inferred relationship Some 4
Hereditary spastic paraplegia Has interpretation True Absent Inferred relationship Some 1
Autosomal dominant hereditary spastic paraplegia Has interpretation True Absent Inferred relationship Some 1
X-linked hereditary spastic paraplegia (disorder) Has interpretation True Absent Inferred relationship Some 3
Autosomal recessive hereditary spastic paraplegia Has interpretation True Absent Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 9B Has interpretation True Absent Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 9A Has interpretation True Absent Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 9B Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 73 Has interpretation True Absent Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 75 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 77 Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 78 (disorder) Has interpretation True Absent Inferred relationship Some 4
Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) Has interpretation True Absent Inferred relationship Some 10
Lethal neonatal spasticity, epileptic encephalopathy syndrome (disorder) Has interpretation True Absent Inferred relationship Some 4

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