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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
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

0 descendants.

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
Chronic progressive 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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