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255314001: Progressive (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
138851000077114 progressif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
380497019 Progressive en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
411831000077116 progressif (valeur de l'attribut) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
646336011 Progressive (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
progressif est un(e) (attribut) descripteurs de comportement true Inferred relationship Some
progressif est un(e) (attribut) chronique true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive spastic paraplegia type 21 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 43 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 62 évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 45 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
paraplégie spastique autosomique récessive type 67 évolution clinique (attribut) True progressif Inferred relationship Some 3
paraplégie spastique autosomique récessive type 59 évolution clinique (attribut) True progressif Inferred relationship Some 3
paraplégie spastique héréditaire (trouble) évolution clinique (attribut) True progressif Inferred relationship Some 2
Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 39 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
X-linked spastic paraplegia type 2 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 36 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 4 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 44 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 46 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 53 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 54 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 32 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 26 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 23 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 64 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 63 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 61 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Spastic paraplegia with Paget disease of bone syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
paraplégie spastique autosomique récessive type 18 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 25 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 10 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 6 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Spastic paraplegia with precocious puberty syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 29 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Spastic paraplegia, nephritis, deafness syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 11 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Spastic paraplegia type 7 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Macrocephaly with spastic paraplegia and dysmorphism syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 6
Spastic paraplegia, glaucoma, intellectual disability syndrome évolution clinique (attribut) True progressif Inferred relationship Some 3
Severe intellectual disability and progressive spastic paraplegia évolution clinique (attribut) True progressif Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 27 évolution clinique (attribut) True progressif Inferred relationship Some 2
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 3 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 69 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 71 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal spastic paraplegia type 72 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 60 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 66 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 14 évolution clinique (attribut) True progressif Inferred relationship Some 3
Hereditary sensory and autonomic neuropathy due to TECPR2 mutation évolution clinique (attribut) True progressif Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 38 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
X-linked spastic paraplegia type 16 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 13 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 56 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 24 évolution clinique (attribut) True progressif Inferred relationship Some 3
X-linked complex hereditary spastic paraplegia évolution clinique (attribut) True progressif Inferred relationship Some 3
X-linked pure hereditary spastic paraplegia évolution clinique (attribut) True progressif Inferred relationship Some 3
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome évolution clinique (attribut) True progressif Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 78 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome évolution clinique (attribut) True progressif Inferred relationship Some 5
Intellectual disability, spasticity, ectrodactyly syndrome évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 9A évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 9B évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 9B évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 73 évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 75 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 77 évolution clinique (attribut) True progressif Inferred relationship Some 2
Childhood-onset nemaline myopathy évolution clinique (attribut) True progressif Inferred relationship Some 2
Intermediate nemaline myopathy évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant amyotrophic lateral sclerosis type 1 évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive amyotrophic lateral sclerosis type 1 évolution clinique (attribut) True progressif Inferred relationship Some 2
Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 6
Proximal myopathy with focal depletion of mitochondria évolution clinique (attribut) True progressif Inferred relationship Some 1
Amyotrophic lateral sclerosis type 1 évolution clinique (attribut) True progressif Inferred relationship Some 2
Juvenile amyotrophic lateral sclerosis type 2 évolution clinique (attribut) True progressif Inferred relationship Some 1
Juvenile amyotrophic lateral sclerosis (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Amyotrophic lateral sclerosis type 3 évolution clinique (attribut) True progressif Inferred relationship Some 1
Juvenile amyotrophic lateral sclerosis type 5 évolution clinique (attribut) True progressif Inferred relationship Some 1
Amyotrophic lateral sclerosis type 6 évolution clinique (attribut) True progressif Inferred relationship Some 2
Amyotrophic lateral sclerosis type 7 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Amyotrophic lateral sclerosis type 8 évolution clinique (attribut) True progressif Inferred relationship Some 2
Amyotrophic lateral sclerosis type 9 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Severe oculo-renal-cerebellar syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Amyotrophic lateral sclerosis type 10 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Familial infantile bilateral striatal necrosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Progressive cerebello-cerebral atrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Spinocerebellar ataxia type 42 évolution clinique (attribut) True progressif Inferred relationship Some 3
Spinocerebellar ataxia type 41 évolution clinique (attribut) True progressif Inferred relationship Some 3
Spinocerebellar ataxia type 43 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Multiple mitochondrial dysfunctions syndrome type 4 évolution clinique (attribut) True progressif Inferred relationship Some 4
ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement évolution clinique (attribut) True progressif Inferred relationship Some 3
Toxic maculopathy due to antimalarial drug évolution clinique (attribut) True progressif Inferred relationship Some 3
Odontoleukodystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Progressive myoclonic epilepsy type 7 évolution clinique (attribut) True progressif Inferred relationship Some 1
encéphalomyélite rubéoleuse congénitale progressive évolution clinique (attribut) True progressif Inferred relationship Some 3
Hyperostosis cranialis interna (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 5
Progressive scapulohumeroperoneal distal myopathy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Cerebellar ataxia with oculomotor apraxia type 4 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Phospholipase A2 activating protein-associated neurodevelopmental disorder (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Severe myopia, generalized joint laxity, short stature syndrome évolution clinique (attribut) True progressif Inferred relationship Some 5
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Autosomal dominant mitochondrial myopathy with exercise intolerance évolution clinique (attribut) True progressif Inferred relationship Some 1
Early-onset calcifying leucoencephalopathy, skeletal dysplasia évolution clinique (attribut) True progressif Inferred relationship Some 4
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1

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