FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

363847004: Movement observable (observable entity)


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
486976015 Movement observable en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
770030010 Movement observable (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


18 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Movement observable Is a Neurological observable true Inferred relationship Some

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

Start Previous Page 11 of 14 Next End


Reference Sets

Description inactivation indicator reference set

Back to Start