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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
Progressive peripheral pterygium of right eye évolution clinique (attribut) True progressif Inferred relationship Some 3
Progressive peripheral pterygium of left eye (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Progressive peripheral pterygium of bilateral eyes (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 5
Peripheral pterygium, progressive évolution clinique (attribut) True progressif Inferred relationship Some 2
Necrobiotic xanthogranuloma (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Necrobiotic xanthogranuloma with paraproteinemia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant Robinow syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal recessive Robinow syndrome évolution clinique (attribut) True progressif Inferred relationship Some 1
Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Bilateral Madelung deformity (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 7
Congenital muscular dystrophy type 1D large gene mutation (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive avascular necrosis of bilateral lunate bones (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Liver cirrhosis due to classical cystic fibrosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Mesomelic dysplasia of upper limb (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive nodular fibrosis of skin évolution clinique (attribut) True progressif Inferred relationship Some 2
Porokeratosis of Mibelli évolution clinique (attribut) True progressif Inferred relationship Some 3
Giant porokeratosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Congenital cataract with ataxia and deafness syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Chronic progressive epilepsia partialis continua of childhood évolution clinique (attribut) True progressif Inferred relationship Some 2
Chronic progressive epilepsia partialis continua évolution clinique (attribut) True progressif Inferred relationship Some 1
Primary biliary cholangitis évolution clinique (attribut) True progressif Inferred relationship Some 5
atrophie cérébrale et cérébelleuse infantile avec microcéphalie postnatale progressive évolution clinique (attribut) True progressif Inferred relationship Some 4
Progressive cerebellar ataxia with hypogonadism évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive familial intrahepatic cholestasis type 2 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive intrahepatic cholestasis évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive familial intrahepatic cholestasis type 1 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal dominant progressive external ophthalmoplegia type 4 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal dominant progressive external ophthalmoplegia type 1 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal dominant progressive external ophthalmoplegia type 5 évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal dominant progressive external ophthalmoplegia type 3 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal recessive Emery-Dreifuss muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
X-linked Emery-Dreifuss muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive supranuclear palsy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Atypical progressive supranuclear palsy syndrome évolution clinique (attribut) True progressif Inferred relationship Some 3
Progressive supranuclear palsy corticobasal syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Progressive supranuclear palsy parkinsonism syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Progressive supranuclear palsy progressive non fluent aphasia évolution clinique (attribut) True progressif Inferred relationship Some 3
Progressive post haemorrhagic ventricular dilatation évolution clinique (attribut) True progressif Inferred relationship Some 3
Diaphyseal dysplasia évolution clinique (attribut) True progressif Inferred relationship Some 3
2-methyl-3-hydroxybutyric aciduria (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder évolution clinique (attribut) True progressif Inferred relationship Some 3
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Childhood-onset basal ganglia degeneration syndrome évolution clinique (attribut) True progressif Inferred relationship Some 2
Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome évolution clinique (attribut) True progressif Inferred relationship Some 4
Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome évolution clinique (attribut) True progressif Inferred relationship Some 1
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome évolution clinique (attribut) True progressif Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 76 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation évolution clinique (attribut) True progressif Inferred relationship Some 2
Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Adenylosuccinate synthetase-like 1-related distal myopathy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
POGLUT1-related limb girdle muscular dystrophy R21 évolution clinique (attribut) True progressif Inferred relationship Some 3
Deafness with epiphyseal dysplasia and short stature syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 5
syndrome de déficience intellectuelle sévère-microcéphalie postnatale progressive-stéréotypies manuelles sur la ligne médiane évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome évolution clinique (attribut) True progressif Inferred relationship Some 3
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Pontine autosomal dominant microangiopathy with leukoencephalopathy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Myotonic dystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Proximal myotonic myopathy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
dystrophie myotonique congénitale évolution clinique (attribut) True progressif Inferred relationship Some 2
Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
LIMS2-related limb girdle muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Primary hyperplasia of mandibular condyle (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Progressive familial intrahepatic cholestasis type 3 évolution clinique (attribut) True progressif Inferred relationship Some 1
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Integral membrane protein 2B related amyloidosis (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Progressive nodular histiocytosis évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 74 évolution clinique (attribut) True progressif Inferred relationship Some 1
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome évolution clinique (attribut) True progressif Inferred relationship Some 2
Spastic paraplegia, severe developmental delay, epilepsy syndrome évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal dominant hereditary spastic paraplegia évolution clinique (attribut) True progressif Inferred relationship Some 2
X-linked hereditary spastic paraplegia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive hereditary spastic paraplegia évolution clinique (attribut) True progressif Inferred relationship Some 2
Pure hereditary spastic paraplegia évolution clinique (attribut) True progressif Inferred relationship Some 2
Complicated hereditary spastic paraplegia évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 17 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 5
Allan-Herndon-Dudley syndrome évolution clinique (attribut) True progressif Inferred relationship Some 7
Infantile ascending hereditary spastic paralysis (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 58 évolution clinique (attribut) True progressif Inferred relationship Some 3
paraplégie spastique autosomique récessive type 70 évolution clinique (attribut) True progressif Inferred relationship Some 3
paraplégie spastique autosomique dominante type 31 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 41 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 42 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 48 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 37 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
X-linked spastic paraplegia type 34 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 5A évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 12 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 19 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 28 évolution clinique (attribut) True progressif Inferred relationship Some 3
paraplégie spastique autosomique type 30 évolution clinique (attribut) True progressif Inferred relationship Some 2
Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Spastic paraplegia, facial cutaneous lesion syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 15 évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 35 évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 21 évolution clinique (attribut) True progressif Inferred relationship Some 3

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