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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
Diplegic cerebral palsy Has interpretation True Absent Inferred relationship Some 5
Athetoid cerebral palsy Has interpretation True Absent Inferred relationship Some 5
Facial palsy as birth trauma Has interpretation True Absent Inferred relationship Some 4
Monoplegic cerebral palsy affecting upper limb (disorder) Has interpretation True Absent Inferred relationship Some 4
Monoplegic cerebral palsy affecting lower limb Has interpretation True Absent Inferred relationship Some 4
Dyskinetic cerebral palsy Has interpretation True Absent Inferred relationship Some 5
Ataxic cerebral palsy Has interpretation True Absent Inferred relationship Some 5
Paraplegic cerebral palsy (disorder) Has interpretation True Absent Inferred relationship Some 4
Non-spastic cerebral palsy (disorder) Has interpretation True Absent Inferred relationship Some 5
Dystonic cerebral palsy (disorder) Has interpretation True Absent Inferred relationship Some 5
Choreic cerebral palsy Has interpretation True Absent Inferred relationship Some 5
Chorea-athetoid cerebral palsy Has interpretation True Absent Inferred relationship Some 5
Mixed cerebral palsy Has interpretation True Absent Inferred relationship Some 3
Bilateral cerebral palsy Has interpretation True Absent Inferred relationship Some 3
Triplegic cerebral palsy (disorder) Has interpretation True Absent Inferred relationship Some 5
Pentaplegic cerebral palsy Has interpretation True Absent Inferred relationship Some 4
Horizontal gaze palsy with progressive scoliosis Has interpretation True Absent Inferred relationship Some 5
Paralytic syndrome of two limbs Has interpretation True Absent Inferred relationship Some 2
Paralytic syndrome of three limbs Has interpretation True Absent Inferred relationship Some 2
Paralytic syndrome on both sides of the body (disorder) Has interpretation True Absent Inferred relationship Some 2
Infantile ascending hereditary spastic paralysis (disorder) Has interpretation True Absent Inferred relationship Some 4
Ophthalmoplegia due to Graves' disease Has interpretation True Absent Inferred relationship Some 5
Acute paralytic poliomyelitis Has interpretation True Absent Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 58 Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 70 (disorder) Has interpretation True Absent Inferred relationship Some 4
Spinal atrophy, ophthalmoplegia, pyramidal syndrome Has interpretation True Absent Inferred relationship Some 3
Erb Duchenne palsy with neuroma due to birth trauma (disorder) Has interpretation True Absent Inferred relationship Some 7
Autosomal dominant spastic paraplegia type 31 (disorder) Has interpretation True Absent Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 41 (disorder) Has interpretation True Absent Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 42 Has interpretation True Absent Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 48 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 37 (disorder) Has interpretation True Absent Inferred relationship Some 2
X-linked spastic paraplegia type 34 Has interpretation True Absent Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 5A Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 12 (disorder) Has interpretation True Absent Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 19 Has interpretation True Absent Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 28 Has interpretation True Absent Inferred relationship Some 2
Autosomal spastic paraplegia type 30 (disorder) Has interpretation True Absent Inferred relationship Some 3
Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder) Has interpretation True Absent Inferred relationship Some 2
Spastic paraplegia, facial cutaneous lesion syndrome (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 15 Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 35 Has interpretation True Absent Inferred relationship Some 4
Progressive external ophthalmoplegia, myopathy, emaciation syndrome Has interpretation True Absent Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 21 Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 43 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 62 Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 45 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 67 (disorder) Has interpretation True Absent Inferred relationship Some 4
Benign nocturnal alternating hemiplegia of childhood Has interpretation True Absent Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 59 Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant progressive external ophthalmoplegia (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive progressive external ophthalmoplegia Has interpretation True Absent Inferred relationship Some 4
External ophthalmoplegia Has interpretation True Absent Inferred relationship Some 4
Progressive external ophthalmoplegia Has interpretation True Absent Inferred relationship Some 4
SPOAN and SPOAN-related disorder Has interpretation True Absent Inferred relationship Some 5
Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder) Has interpretation True Absent Inferred relationship Some 7
Autosomal recessive spastic paraplegia type 39 (disorder) Has interpretation True Absent Inferred relationship Some 4
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) Has interpretation True Absent Inferred relationship Some 10
Flaccid diplegia of upper limbs (disorder) Has interpretation True Absent Inferred relationship Some 2
Spastic diplegia of upper limbs (disorder) Has interpretation True Absent Inferred relationship Some 2
Diplegia of lower limbs (disorder) Has interpretation True Absent Inferred relationship Some 2
Spastic monoplegia of upper limb (disorder) Has interpretation True Absent Inferred relationship Some 2
Spastic monoplegia of lower limb (disorder) Has interpretation True Absent Inferred relationship Some 2
Erb Duchenne palsy with neuropraxis due to traction birth trauma (disorder) Has interpretation True Absent Inferred relationship Some 5
Macrostomia, preauricular tag, external ophthalmoplegia syndrome (disorder) Has interpretation True Absent Inferred relationship Some 5
Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome (disorder) Has interpretation True Absent Inferred relationship Some 6
X-linked spastic paraplegia type 2 (disorder) Has interpretation True Absent Inferred relationship Some 7
Autosomal dominant spastic paraplegia type 36 (disorder) Has interpretation True Absent Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 4 (disorder) Has interpretation True Absent Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 44 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 46 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 53 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 54 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 55 (disorder) Has interpretation True Absent Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 57 (disorder) Has interpretation True Absent Inferred relationship Some 3
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Has interpretation True Absent Inferred relationship Some 6
Functional monoparesis (disorder) Has interpretation True Absent Inferred relationship Some 4
Functional paraparesis (disorder) Has interpretation True Absent Inferred relationship Some 2
Functional hemiparesis (disorder) Has interpretation True Absent Inferred relationship Some 3
Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder) Has interpretation True Absent Inferred relationship Some 3
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (disorder) Has interpretation True Absent Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 32 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 26 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 23 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 64 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 63 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 61 (disorder) Has interpretation True Absent Inferred relationship Some 4
Spastic paraplegia with Paget disease of bone syndrome (disorder) Has interpretation True Absent Inferred relationship Some 1
Autosomal recessive spastic paraplegia type 18 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 25 (disorder) Has interpretation True Absent Inferred relationship Some 4
Autosomal dominant spastic paraplegia type 10 (disorder) Has interpretation True Absent Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 6 (disorder) Has interpretation True Absent Inferred relationship Some 2
Spastic paraplegia with precocious puberty syndrome (disorder) Has interpretation True Absent Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 29 (disorder) Has interpretation True Absent Inferred relationship Some 2
Spastic paraplegia, nephritis, deafness syndrome (disorder) Has interpretation True Absent Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 11 (disorder) Has interpretation True Absent Inferred relationship Some 4
Spastic paraplegia type 7 (disorder) Has interpretation True Absent Inferred relationship Some 5
Macrocephaly with spastic paraplegia and dysmorphism syndrome (disorder) Has interpretation True Absent Inferred relationship Some 7
Congenital suprabulbar paresis (disorder) Has interpretation True Absent Inferred relationship Some 3
Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome (disorder) Has interpretation True Absent Inferred relationship Some 6
Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder) Has interpretation True Absent Inferred relationship Some 4

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