702322003: Non-progressive (qualifier value)

SNOMED CT Concept\Qualifier value (qualifier value)\...

\Special atomic mapping values\Special disorder atoms\Courses\Non-progressive

\Descriptor (qualifier value)\Time patterns\Courses\Non-progressive

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2995210017 Non-progressive en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2995437018 Non-progressive (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Non-progressive	Is a	Courses	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Congenital quadriplegia	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of spastic cerebral palsy affecting the lower half of the body, including both legs.	Clinical course	True	Non-progressive	Inferred relationship	Some	2
Monoplegic cerebral palsy affecting upper limb	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of spastic cerebral palsy affecting all four limbs; the term bilateral hemiplegia may also be used when one side has a significantly different tone compared with the other.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
Monoplegic cerebral palsy affecting lower limb	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of spastic cerebral palsy affecting the arm and/or leg on one side of the body. An ipsilateral upper and/or lower extremity is affected.	Clinical course	True	Non-progressive	Inferred relationship	Some	2
A form of non-spastic cerebral palsy with decreased muscle tone, noticeably floppy muscles with poor or no head control.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of athetoid cerebral palsy with bilateral involuntary movements.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
Cerebral palsy, not congenital or infantile, acute	Clinical course	True	Non-progressive	Inferred relationship	Some	2
A subtype of non-spastic cerebral palsy with involuntary, uncontrolled recurring, and occasionally stereotyped movements with a varying muscle tone; primitive reflex patterns predominate.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of spastic cerebral palsy affecting only one limb	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of spastic cerebral palsy affecting two limbs; usually the legs are affected more than the arms.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A type of cerebral palsy defined by increased tone and pathological reflexes resulting in an abnormal pattern of movement and posture.	Clinical course	True	Non-progressive	Inferred relationship	Some	2
Spastic tetraplegia with rigidity syndrome	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A subtype of non-spastic cerebral palsy with loss of muscular coordination with abnormal force and rhythm, and impairment of accuracy; commonly presents with gait and trunk ataxia, poor balance, past pointing, terminal intention tremor, scanning speech, nystagmus and other abnormal eye movements, and hypotonia. Low tone is a prominent feature.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of dyskinetic cerebral palsy with slow, writhing movements that are often repetitive, sinuous, and rhythmic.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
Dystonic/rigid cerebral palsy	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain.	Clinical course	True	Non-progressive	Inferred relationship	Some	1
A less common type of cerebral palsy defined by decreased and/or fluctuating muscle tone; multiple forms of non-spastic cerebral palsy are each characterized by particular impairments; one of the main characteristics of non-spastic cerebral palsy is involuntary movement. Subtypes include ataxic and dyskinetic forms.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of dyskinetic cerebral palsy with involuntary movements accompanied by an abnormal, sustained posture.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
Choreic cerebral palsy	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of dyskinetic cerebral palsy with a combination of chorea and athetosis; movements are irregular, but twisting and curving.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of cerebral palsy where no predominant motion can be determined; when it is a mixed CP form, i.e. spasticity with ataxia and/or dyskinesia, the child should be classified according to the dominant clinical feature	Clinical course	True	Non-progressive	Inferred relationship	Some	2
A form of spastic cerebral palsy affecting both sides of the body; the Surveillance of Cerebral Palsy in Europe (SCPE) does not recommend the use of diplegia/quadriplegia terms, and recommends using instead the term bilateral spastic cerebral palsy and subtypes.	Clinical course	True	Non-progressive	Inferred relationship	Some	2
A form of spastic cerebral palsy affecting three limbs; this could be both arms and a leg, or both legs and an arm. In some instances, it has referred to one upper and one lower extremity and the face.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
A form of spastic cerebral palsy affecting all four limbs with neck and head paralysis, often accompanied by eating and breathing complications.	Clinical course	True	Non-progressive	Inferred relationship	Some	2
Worster-Drought syndrome (WDS) is a form of cerebral palsy characterized by congenital pseudobulbar (suprabulbar) paresis manifesting as selective weakness of the lips, tongue and soft palate, dysphagia, dysphonia, drooling and jaw jerking.	Clinical course	True	Non-progressive	Inferred relationship	Some	2
A rare, genetic, autosomal recessive cerebellar ataxia disease characterized by nonprogressive cerebellar ataxia, with onset in infancy, manifesting with delayed motor and speech development, gait ataxia, dysmetria, hypotonia, increased deep tendon reflexes, and dysarthria. Additional variable manifestations include moderate nystagmus on lateral gaze, mild spasticity, intention tremor, short stature and pes planus. Brain imaging reveals cerebellar vermis atrophy.	Clinical course	True	Non-progressive	Inferred relationship	Some	2
A rare, multiple congenital anomalies/dysmorphic syndrome characterized by craniofacial dysmorphism, including microbrachycephaly, sloping forehead, micro/anophthalmia, large ears, prominent nasal root, mild micrognathia, and cleft palate, associated with cerebral palsy with choreoathetoid movements, intellectual disability, dextrocardia and longitudinal folding of plantae pedis. There have been no further descriptions in the literature since 1992.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
Congenital non-progressive ataxia	Clinical course	True	Non-progressive	Inferred relationship	Some	2
Non-progressive hereditary glomerulonephritis (disorder)	Clinical course	True	Non-progressive	Inferred relationship	Some	2
A rare autosomal recessive cerebellar ataxia characterized by early onset of non- or slowly progressive cerebellar signs and symptoms including truncal and gait ataxia, dysarthria, dysmetria, dysdiadochokinesis, tremor, and nystagmus. Delayed psychomotor development and intellectual disability are variable. Additional reported features are spasticity, hypotonia, cataracts, and sensorineural hearing loss, among others. Brain imaging shows cerebellar atrophy.	Clinical course	True	Non-progressive	Inferred relationship	Some	2
X-linked non progressive cerebellar ataxia is a rare hereditary ataxia characterized by delayed early motor development, severe neonatal hypotonia, non-progressive ataxia and slow eye movements, presenting normal cognitive abilities and absence of pyramidal signs. Frequently patients also manifest intention tremor, mild dysphagia, and dysarthria. Brain MRI reveals global cerebellar atrophy with absence of other malformations or degenerations of the central and peripheral nervous systems.	Clinical course	True	Non-progressive	Inferred relationship	Some	1
Peripheral pterygium, stationary	Clinical course	True	Non-progressive	Inferred relationship	Some	2
Stationary peripheral pterygium of right eye (disorder)	Clinical course	True	Non-progressive	Inferred relationship	Some	3
Stationary peripheral pterygium of left eye	Clinical course	True	Non-progressive	Inferred relationship	Some	3
Stationary peripheral pterygium of bilateral eyes (disorder)	Clinical course	True	Non-progressive	Inferred relationship	Some	5
A rare mitochondrial disease characterized by a distinctive MRI pattern of cavitating leukodystrophy, predominantly in the posterior region of the cerebral hemispheres. The clinical picture varies widely between acute neurometabolic decompensation in infancy with loss of developmental milestones, seizures, and pyramidal signs rapidly evolving into spastic tetraparesis, to subtle neurological symptoms presenting in adolescence. The disease course tends to stabilize over time in most patients, and marked recovery of milestones may be observed.	Clinical course	True	Non-progressive	Inferred relationship	Some	3
Congenital insensitivity to pain with severe intellectual disability is a rare autosomal recessive hereditary sensory and autonomic neuropathy characterized by the complete absence of pain perception from birth, an unresponsiveness to soft touch, severe non-progressive cognitive delay, and normal motor movement/behavior and strength. Affected cases retained hot and cold perception.	Clinical course	True	Non-progressive	Inferred relationship	Some	6
Dysequilibrium syndrome (DES) is a non-progressive cerebellar disorder characterized by ataxia associated with an intellectual disability, delayed ambulation and cerebellar hypoplasia.	Clinical course	True	Non-progressive	Inferred relationship	Some	4
Non-progressive cerebellar ataxia	Clinical course	True	Non-progressive	Inferred relationship	Some	1
Non-progressive atrophy of muscle (disorder)	Clinical course	True	Non-progressive	Inferred relationship	Some	2

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
2995210017	Non-progressive	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2995437018	Non-progressive (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core