255314001: Progressive (qualifier value)

SNOMED CT Concept\valeur de l'attribut\...

\valeurs d'attributs spéciaux\éléments particuliers d'un trouble\évolution\chronique\progressif

\descripteur\caractéristiques temporelles\évolution\chronique\progressif
\descripteur\descripteurs de comportement\progressif

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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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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