255314001: Progressive (qualifier value)

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:

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
141971000052119 progressiv sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

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
Autosomal recessive spastic paraplegia type 63 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 61 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Spastic paraplegia with Paget disease of bone syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 18 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 25 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 10 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 6 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Spastic paraplegia with precocious puberty syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 29 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Spastic paraplegia, nephritis, deafness syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Autosomal recessive spastic paraplegia type 11 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Spastic paraplegia type 7 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Macrocephaly with spastic paraplegia and dysmorphism syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	6
Spastic paraplegia, glaucoma, intellectual disability syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Severe intellectual disability and progressive spastic paraplegia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Autosomal recessive spastic paraplegia type 27	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 3 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 69	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 71	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal spastic paraplegia type 72	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 60	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 66	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 14	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Hereditary sensory and autonomic neuropathy due to TECPR2 mutation	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	6
Autosomal dominant spastic paraplegia type 38 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
X-linked spastic paraplegia type 16 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 13 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 56 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive spastic paraplegia type 24	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
X-linked complex hereditary spastic paraplegia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
X-linked pure hereditary spastic paraplegia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	6
Autosomal recessive spastic paraplegia type 78 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Intellectual disability, spasticity, ectrodactyly syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Autosomal dominant spastic paraplegia type 9A	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant spastic paraplegia type 9B	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 9B	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant spastic paraplegia type 73	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 75 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive spastic paraplegia type 77	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Childhood-onset nemaline myopathy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Intermediate nemaline myopathy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal dominant amyotrophic lateral sclerosis type 1	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive amyotrophic lateral sclerosis type 1	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Bilateral hip and radial head dislocations, short stature, scoliosis, carpal coalition, pes cavus, facial dysmorphism syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	6
Proximal myopathy with focal depletion of mitochondria	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Amyotrophic lateral sclerosis type 1	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Juvenile amyotrophic lateral sclerosis type 2	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Juvenile amyotrophic lateral sclerosis (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Amyotrophic lateral sclerosis type 3	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Juvenile amyotrophic lateral sclerosis type 5	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Amyotrophic lateral sclerosis type 6	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Amyotrophic lateral sclerosis type 7 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Amyotrophic lateral sclerosis type 8	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Amyotrophic lateral sclerosis type 9 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Severe oculo-renal-cerebellar syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Amyotrophic lateral sclerosis type 10 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Familial infantile bilateral striatal necrosis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Progressive cerebello-cerebral atrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Spinocerebellar ataxia type 42	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Spinocerebellar ataxia type 41	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Spinocerebellar ataxia type 43 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Multiple mitochondrial dysfunctions syndrome type 4	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Toxic maculopathy due to antimalarial drug	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Odontoleukodystrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Progressive myoclonic epilepsy type 7	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Progressive congenital rubella encephalomyelitis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Hyperostosis cranialis interna (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Progressive scapulohumeroperoneal distal myopathy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Cerebellar ataxia with oculomotor apraxia type 4 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Phospholipase A2 activating protein-associated neurodevelopmental disorder (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Severe myopia, generalized joint laxity, short stature syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Autosomal dominant mitochondrial myopathy with exercise intolerance	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Early-onset calcifying leucoencephalopathy, skeletal dysplasia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Polyglucosan body myopathy type 2	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive myoclonic epilepsy type 9	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Spondyloepiphyseal dysplasia Stanescu type	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
PCNA-related progressive neurodegenerative photosensitivity syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Severe early-onset pulmonary alveolar proteinosis due to methionyl-transfer ribonucleic acid synthetase 1 deficiency (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Leukocyte chemotactic factor-2 amyloidosis (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Corticobasal syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Megaconial congenital muscular dystrophy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Distal hereditary motor neuropathy type 2 (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	1
Goldmann-Favre syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Smoldering systemic mastocytosis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Limb girdle muscular dystrophy due to POMK deficiency	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Progressive macular hypomelanosis	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Night blindness, skeletal anomalies, dysmorphism syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	3
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
PYCR2-related microcephaly, progressive leucoencephalopathy	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	5
Osteosclerotic metaphyseal dysplasia	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2
Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	4
Sorsby pseudoinflammatory fundus dystrophy (disorder)	Clinical course	True	Progressive (qualifier value)	Inferred relationship	Some	2

Start Previous Page 6 of 7 End

This concept is not in any reference sets

Back to Start

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
141971000052119	progressiv	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)