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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
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Young adult-onset distal hereditary motor neuropathy évolution clinique (attribut) True progressif Inferred relationship Some 2
syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
maladie de Charcot-Marie-Tooth autosomique dominante type 2Q évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
syndrome neurodégénératif sévère avec lipodystrophie évolution clinique (attribut) True progressif Inferred relationship Some 3
Childhood-onset spasticity with hyperglycinemia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Progressive retinal dystrophy due to retinol transport defect (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
X-linked myopathy with postural muscle atrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Fatal post-viral neurodegenerative disorder évolution clinique (attribut) True progressif Inferred relationship Some 4
syndrome d'hyperuricémie, hypertension artérielle pulmonaire, insuffisance rénale, alcalose évolution clinique (attribut) True progressif Inferred relationship Some 2
Mills syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
hyperphosphatasemia tarda évolution clinique (attribut) True progressif Inferred relationship Some 5
dysplasie épiphysaire multiple type Al-Gazali évolution clinique (attribut) True progressif Inferred relationship Some 2
Pyknodysostosis évolution clinique (attribut) True progressif Inferred relationship Some 2
Osteopetrosis - delayed type évolution clinique (attribut) True progressif Inferred relationship Some 3
Infantile malignant osteopetrosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Sclerosteosis évolution clinique (attribut) True progressif Inferred relationship Some 2
Muscle eye brain disease with bilateral multicystic leukodystrophy évolution clinique (attribut) True progressif Inferred relationship Some 6
Progressive myoclonic epilepsy type 6 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 1
Adult-onset autosomal recessive cerebellar ataxia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Axial osteosclerosis évolution clinique (attribut) True progressif Inferred relationship Some 5
myopathie distale précoce type Laing évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 8 évolution clinique (attribut) True progressif Inferred relationship Some 2
Thoracic dysplasia and hydrocephalus syndrome évolution clinique (attribut) True progressif Inferred relationship Some 3
Endosteal hyperostoses évolution clinique (attribut) True progressif Inferred relationship Some 2
Distal myopathy with anterior tibial onset évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Endosteal hyperostoses with cerebellar hypoplasia évolution clinique (attribut) True progressif Inferred relationship Some 4
Dysplasia of head of femur Meyer type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Oculopharyngeal muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive limb girdle muscular dystrophy type 2D (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2A (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
maladie de Huntington évolution clinique (attribut) True progressif Inferred relationship Some 1
Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2O (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2L (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
dystrophie musculaire des ceintures autosomique récessive type 2N évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2M (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Congenital muscular dystrophy with hyperlaxity (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal dominant osteopetrosis type 2 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Pelvic muscular dystrophy évolution clinique (attribut) False progressif Inferred relationship Some 2
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Autosomal dominant adult-onset proximal spinal muscular atrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Distal muscular dystrophy with juvenile onset évolution clinique (attribut) True progressif Inferred relationship Some 3
Dyschondrosteosis and nephritis syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Tibial muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 3
Alpha-B crystallin-related late-onset myopathy évolution clinique (attribut) True progressif Inferred relationship Some 2
Gemignani syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Distal myopathy Welander type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Severe childhood autosomal recessive muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
General paresis - neurosyphilis (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive limb girdle muscular dystrophy type 2S (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
dysplasie en boomerang évolution clinique (attribut) True progressif Inferred relationship Some 3
Autosomal recessive limb girdle muscular dystrophy type 2R (disorder) évolution clinique (attribut) False progressif Inferred relationship Some 2
Atelosteogenesis type 2 évolution clinique (attribut) True progressif Inferred relationship Some 4
Becker muscular dystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Osteosclerosis (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
ADan amyloidosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Nievergelt's syndrome évolution clinique (attribut) True progressif Inferred relationship Some 2
Pseudodiastrophic dysplasia évolution clinique (attribut) True progressif Inferred relationship Some 3
Muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Akinetic-rigid form of Huntington's disease évolution clinique (attribut) True progressif Inferred relationship Some 2
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations évolution clinique (attribut) True progressif Inferred relationship Some 1
SHOX-related short stature évolution clinique (attribut) True progressif Inferred relationship Some 2
Hydrocalycosis évolution clinique (attribut) True progressif Inferred relationship Some 3
Wolcott-Rallison dysplasia évolution clinique (attribut) True progressif Inferred relationship Some 2
Lenz-Majewski hyperostosis syndrome évolution clinique (attribut) True progressif Inferred relationship Some 2
Atelosteogenesis évolution clinique (attribut) True progressif Inferred relationship Some 3
Mesomelic dysplasia Savarirayan type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
dysplasie épiphysaire multiple due à une anomalie du collagène 9 évolution clinique (attribut) True progressif Inferred relationship Some 2
Epiphyseal dysplasia évolution clinique (attribut) True progressif Inferred relationship Some 2
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier évolution clinique (attribut) True progressif Inferred relationship Some 2
Worth disease évolution clinique (attribut) True progressif Inferred relationship Some 4
Lethal Larsen-like syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Erb's muscular dystrophy évolution clinique (attribut) False progressif Inferred relationship Some 2
X-linked scapuloperoneal muscular dystrophy (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Craniometadiaphyseal dysplasia wormian bone type (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 4
Multiple epiphyseal dysplasia with severe proximal femoral dysplasia (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Progressive avascular necrosis of lunate évolution clinique (attribut) True progressif Inferred relationship Some 2
Muscular dystrophy-deafmutism syndrome évolution clinique (attribut) False progressif Inferred relationship Some 2
Congenital muscular dystrophy type 1A évolution clinique (attribut) True progressif Inferred relationship Some 2
Congenital hereditary muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Congenital muscular dystrophy type 1B évolution clinique (attribut) True progressif Inferred relationship Some 2
Autosomal recessive limb girdle muscular dystrophy type 2U évolution clinique (attribut) True progressif Inferred relationship Some 2
Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 3
Fukuyama congenital muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Amyotrophic lateral sclerosis type 4 évolution clinique (attribut) True progressif Inferred relationship Some 2
syndrome de dysplasie ectodermique anhidrotique-immunodéficience-ostéopétrose-lymphoedème évolution clinique (attribut) True progressif Inferred relationship Some 6
Merosin deficient congenital muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
dystrophie musculaire congénitale de Walker-Warburg évolution clinique (attribut) True progressif Inferred relationship Some 3
Muscle-eye-brain disease, congenital muscular dystrophy évolution clinique (attribut) True progressif Inferred relationship Some 2
Distal muscular dystrophy, Miyoshi type évolution clinique (attribut) True progressif Inferred relationship Some 3
Multiple epiphyseal dysplasia type 4 (disorder) évolution clinique (attribut) True progressif Inferred relationship Some 2
Steinert myotonic dystrophy syndrome évolution clinique (attribut) True progressif Inferred relationship Some 2

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