255314001: progressief (kwalificatiewaarde)

SNOMED CT Concept\Qualifier value\...

\Special atomic mapping values\Special disorder atoms\Courses\Chronic\Progressive (qualifier value)

\Descriptor (qualifier value)\Time patterns\Courses\Chronic\Progressive (qualifier value)
\Descriptor (qualifier value)\Behaviour descriptors\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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Progressive (qualifier value)	Is a	Behaviour descriptors	true	Inferred relationship	Some
Progressive (qualifier value)	Is a	Chronic	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
chronische progressieve epilepsia partialis continua	Clinical course	False	Progressive (qualifier value)	Inferred relationship	Some	1
Primary biliary cholangitis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Progressive cerebellar ataxia with hypogonadism	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive familial intrahepatic cholestasis type 2 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive intrahepatic cholestasis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive familial intrahepatic cholestasis type 1 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal dominant progressive external ophthalmoplegia type 4 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal dominant progressive external ophthalmoplegia type 1 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal dominant progressive external ophthalmoplegia type 2 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal dominant progressive external ophthalmoplegia type 5	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal dominant progressive external ophthalmoplegia type 3 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal recessive Emery-Dreifuss muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
X-linked Emery-Dreifuss muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive supranuclear palsy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Atypical progressive supranuclear palsy syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Progressive supranuclear palsy corticobasal syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Progressive supranuclear palsy parkinsonism syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Progressive supranuclear palsy progressive non fluent aphasia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Progressive post haemorrhagic ventricular dilatation	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Diaphyseal dysplasia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
2-methyl-3-hydroxybutyric aciduria (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Childhood-onset basal ganglia degeneration syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Kyphosis, lateral tongue atrophy, myofibrillar myopathy syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Autosomal recessive spastic paraplegia type 76 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Adenylosuccinate synthetase-like 1-related distal myopathy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
POGLUT1-related limb girdle muscular dystrophy R21	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Deafness with epiphyseal dysplasia and short stature syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Pontine autosomal dominant microangiopathy with leukoencephalopathy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Myotonic dystrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Proximal myotonic myopathy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Congenital myotonic dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
LIMS2-related limb girdle muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Primary hyperplasia of mandibular condyle (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive familial intrahepatic cholestasis type 3	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Integral membrane protein 2B related amyloidosis (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Progressive nodular histiocytosis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 74	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Spastic paraplegia, severe developmental delay, epilepsy syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal dominant hereditary spastic paraplegia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
X-linked hereditary spastic paraplegia (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive hereditary spastic paraplegia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Pure hereditary spastic paraplegia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Complicated hereditary spastic paraplegia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant spastic paraplegia type 17 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Allan-Herndon-Dudley syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	7
Infantile ascending hereditary spastic paralysis (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 58	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 70 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 31 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 41 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 42	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 48 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant spastic paraplegia type 37 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
X-linked spastic paraplegia type 34	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 5A	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant spastic paraplegia type 12 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 19	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 28	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal spastic paraplegia type 30 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Spastic paraplegia, facial cutaneous lesion syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 15	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 35	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 21	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 43 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 62	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 45 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 67 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 59	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Hereditary spastic paraplegia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	6
Autosomal recessive spastic paraplegia type 39 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
X-linked spastic paraplegia type 2 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	6
Autosomal dominant spastic paraplegia type 36 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 4 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 44 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 46 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 53 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 54 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 32 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 26 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 23 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 64 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 63 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3

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Id	Description	Lang	Type	Status	Case?	Module
380497019	Progressive	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
646336011	Progressive (qualifier value)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4512401000146118	progressief	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4512411000146116	progressief (kwalificatiewaarde)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4512421000146114	voortschrijdend	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4790281000146113	toenemend	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
13051071000146117	De ziekte neemt toe.	nl	Definition	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14985231000146110	Als de ziekte erger wordt. Bijvoorbeeld als een tumor groeit.	nl	Definition	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)