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255314001: Progressive (qualifier value)

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

Descriptions:

Id Description Lang Type Status Case? Module
380497019 Progressive en Synonym Active Entire term case insensitive SNOMED CT core module
646336011 Progressive (qualifier value) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive Is a Behavior descriptors true Inferred relationship Existential restriction modifier
Progressive Is a Chronic true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive spastic paraplegia type 63 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 61 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Spastic paraplegia with Paget disease of bone syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 18 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 25 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 10 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 6 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Spastic paraplegia with precocious puberty syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 29 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Spastic paraplegia, nephritis, deafness syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 5
Autosomal recessive spastic paraplegia type 11 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Spastic paraplegia type 7 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Macrocephaly with spastic paraplegia and dysmorphism syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 6
Spastic paraplegia, glaucoma, intellectual disability syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Severe intellectual disability and progressive spastic paraplegia Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Autosomal recessive spastic paraplegia type 27 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 3 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 69 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 71 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal spastic paraplegia type 72 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 60 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 66 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 14 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation Clinical course True Progressive Inferred relationship Existential restriction modifier 6
Autosomal dominant spastic paraplegia type 38 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
X-linked spastic paraplegia type 16 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 13 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 56 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 24 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
X-linked complex hereditary spastic paraplegia Clinical course True Progressive Inferred relationship Existential restriction modifier 3
X-linked pure hereditary spastic paraplegia Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 6
Autosomal recessive spastic paraplegia type 78 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 5
Intellectual disability, spasticity, ectrodactyly syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Autosomal dominant spastic paraplegia type 9A Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 9B Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 9B Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 73 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 75 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive spastic paraplegia type 77 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Childhood-onset nemaline myopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Intermediate nemaline myopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal dominant amyotrophic lateral sclerosis type 1 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive amyotrophic lateral sclerosis type 1 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 6
Proximal myopathy with focal depletion of mitochondria Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Amyotrophic lateral sclerosis type 1 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Juvenile amyotrophic lateral sclerosis type 2 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Juvenile amyotrophic lateral sclerosis Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Amyotrophic lateral sclerosis type 3 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Juvenile amyotrophic lateral sclerosis type 5 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Amyotrophic lateral sclerosis type 6 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Amyotrophic lateral sclerosis type 7 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Amyotrophic lateral sclerosis type 8 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Amyotrophic lateral sclerosis type 9 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Severe oculo-renal-cerebellar syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Amyotrophic lateral sclerosis type 10 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Familial infantile bilateral striatal necrosis Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Progressive cerebello-cerebral atrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Spinocerebellar ataxia type 42 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 41 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia type 43 Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Multiple mitochondrial dysfunctions syndrome type 4 Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Toxic maculopathy of bilateral eyes caused by antimalarial drug Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Odontoleukodystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Progressive myoclonic epilepsy type 7 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Progressive congenital rubella encephalomyelitis Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Hyperostosis cranialis interna Clinical course True Progressive Inferred relationship Existential restriction modifier 5
Progressive scapulohumeroperoneal distal myopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Cerebellar ataxia with oculomotor apraxia type 4 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Phospholipase A2 activating protein-associated neurodevelopmental disorder Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Severe myopia, generalized joint laxity, short stature syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 5
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Autosomal dominant mitochondrial myopathy with exercise intolerance Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Early-onset calcifying leukoencephalopathy, skeletal dysplasia Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Polyglucosan body myopathy type 2 Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Progressive myoclonic epilepsy type 9 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Spondyloepiphyseal dysplasia Stanescu type Clinical course True Progressive Inferred relationship Existential restriction modifier 5
Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Leukocyte chemotactic factor-2 amyloidosis Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Corticobasal syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Megaconial congenital muscular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Distal hereditary motor neuropathy type 2 Clinical course True Progressive Inferred relationship Existential restriction modifier 1
Goldmann-Favre syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Smoldering systemic mastocytosis Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Limb girdle muscular dystrophy due to protein O-mannose kinase deficiency Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Progressive macular hypomelanosis Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Night blindness, skeletal anomalies, dysmorphism syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 3
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy Clinical course True Progressive Inferred relationship Existential restriction modifier 5
Osteosclerotic metaphyseal dysplasia Clinical course True Progressive Inferred relationship Existential restriction modifier 2
Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency Clinical course True Progressive Inferred relationship Existential restriction modifier 4
Sorsby pseudoinflammatory fundus dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier 2

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