2667000: afwezig (kwalificatiewaarde)

SNOMED CT Concept\Qualifier value\Finding value (qualifier value)\Absence findings\Absent

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

Descriptions:

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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Reference Sets

Dutch microscopic ordinal test result simple reference set (foundation metadata concept)

Dutch mixed flora finding simple reference set (foundation metadata concept)

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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
4453391000146111	afwezig	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4453401000146114	afwezig (kwalificatiewaarde)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4453411000146111	niet aanwezig	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4453421000146118	afwezigheid van	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)