FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

255314001: Progressive (qualifier value)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progressive Is a Behaviour descriptors true Inferred relationship Some
Progressive Is a Chronic true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Autosomal recessive spastic paraplegia type 15 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 35 Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 21 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 43 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 62 Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 45 Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 67 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 59 Clinical course True Progressive Inferred relationship Some 3
Hereditary spastic paraplegia Clinical course True Progressive Inferred relationship Some 2
Hereditary sensory and autonomic neuropathy with spastic paraplegia Clinical course True Progressive Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 39 Clinical course True Progressive Inferred relationship Some 3
Spastic paraplegia type 2 Clinical course True Progressive Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 36 Clinical course True Progressive Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 4 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 44 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 46 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 53 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 54 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 32 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 26 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 23 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 64 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 63 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 61 Clinical course True Progressive Inferred relationship Some 3
Spastic paraplegia with Paget disease of bone syndrome Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 18 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 25 Clinical course True Progressive Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 10 Clinical course True Progressive Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 6 Clinical course True Progressive Inferred relationship Some 3
Spastic paraplegia with precocious puberty syndrome Clinical course True Progressive Inferred relationship Some 1
Autosomal dominant spastic paraplegia type 29 Clinical course True Progressive Inferred relationship Some 1
Spastic paraplegia, nephritis, deafness syndrome Clinical course True Progressive Inferred relationship Some 5
Autosomal recessive spastic paraplegia type 11 Clinical course True Progressive Inferred relationship Some 3
Spastic paraplegia type 7 Clinical course True Progressive Inferred relationship Some 3
Fryns macrocephaly Clinical course True Progressive Inferred relationship Some 6
Spastic paraplegia, glaucoma, intellectual disability syndrome Clinical course True Progressive Inferred relationship Some 3
Severe intellectual disability and progressive spastic paraplegia Clinical course True Progressive Inferred relationship Some 4
Autosomal recessive spastic paraplegia type 27 Clinical course True Progressive Inferred relationship Some 2
MT-ATP6-related mitochondrial spastic paraplegia Clinical course True Progressive Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 3 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 69 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 71 Clinical course True Progressive Inferred relationship Some 3
Autosomal spastic paraplegia type 72 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 60 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 66 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 14 Clinical course True Progressive Inferred relationship Some 3
Hereditary sensory and autonomic neuropathy due to TECPR2 mutation Clinical course True Progressive Inferred relationship Some 6
Autosomal dominant spastic paraplegia type 38 Clinical course True Progressive Inferred relationship Some 3
X-linked spastic paraplegia type 16 Clinical course True Progressive Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 13 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 56 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive spastic paraplegia type 24 Clinical course True Progressive Inferred relationship Some 3
X-linked complex hereditary spastic paraplegia Clinical course True Progressive Inferred relationship Some 3
X-linked pure hereditary spastic paraplegia Clinical course True Progressive Inferred relationship Some 3
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome Clinical course True Progressive Inferred relationship Some 6
Autosomal recessive spastic paraplegia type 78 Clinical course True Progressive Inferred relationship Some 3
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction Clinical course True Progressive Inferred relationship Some 4
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome Clinical course True Progressive Inferred relationship Some 5
Intellectual disability, spasticity, ectrodactyly syndrome Clinical course True Progressive Inferred relationship Some 3
Autosomal dominant spastic paraplegia type 9A Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 9B Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 9B Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant spastic paraplegia type 73 Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 75 Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive spastic paraplegia type 77 Clinical course True Progressive Inferred relationship Some 2
Childhood-onset nemaline myopathy Clinical course True Progressive Inferred relationship Some 2
Intermediate nemaline myopathy Clinical course True Progressive Inferred relationship Some 2
Autosomal dominant amyotrophic lateral sclerosis type 1 Clinical course True Progressive Inferred relationship Some 2
Autosomal recessive amyotrophic lateral sclerosis type 1 Clinical course True Progressive Inferred relationship Some 2
Steel syndrome Clinical course True Progressive Inferred relationship Some 6
Proximal myopathy with focal depletion of mitochondria Clinical course True Progressive Inferred relationship Some 1
Amyotrophic lateral sclerosis type 1 Clinical course True Progressive Inferred relationship Some 2
Juvenile amyotrophic lateral sclerosis type 2 Clinical course True Progressive Inferred relationship Some 1
Juvenile amyotrophic lateral sclerosis Clinical course True Progressive Inferred relationship Some 2
Amyotrophic lateral sclerosis type 3 Clinical course True Progressive Inferred relationship Some 1
Juvenile amyotrophic lateral sclerosis type 5 Clinical course True Progressive Inferred relationship Some 1
Amyotrophic lateral sclerosis type 6 Clinical course True Progressive Inferred relationship Some 2
Amyotrophic lateral sclerosis type 7 Clinical course True Progressive Inferred relationship Some 2
Amyotrophic lateral sclerosis type 8 Clinical course True Progressive Inferred relationship Some 2
Amyotrophic lateral sclerosis type 9 Clinical course True Progressive Inferred relationship Some 2
Severe oculo-renal-cerebellar syndrome Clinical course True Progressive Inferred relationship Some 4
Amyotrophic lateral sclerosis type 10 Clinical course True Progressive Inferred relationship Some 2
Familial infantile bilateral striatal necrosis Clinical course True Progressive Inferred relationship Some 3
Progressive cerebello-cerebral atrophy Clinical course True Progressive Inferred relationship Some 4
Spinocerebellar ataxia type 42 Clinical course True Progressive Inferred relationship Some 3
Spinocerebellar ataxia type 41 Clinical course True Progressive Inferred relationship Some 3
Spinocerebellar ataxia type 43 Clinical course True Progressive Inferred relationship Some 3
Multiple mitochondrial dysfunctions syndrome type 4 Clinical course True Progressive Inferred relationship Some 4
ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement Clinical course True Progressive Inferred relationship Some 3
Toxic maculopathy due to antimalarial drug Clinical course True Progressive Inferred relationship Some 3
Odontoleukodystrophy Clinical course True Progressive Inferred relationship Some 4
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome Clinical course True Progressive Inferred relationship Some 4
Progressive myoclonic epilepsy type 7 Clinical course True Progressive Inferred relationship Some 1
Progressive congenital rubella encephalomyelitis Clinical course True Progressive Inferred relationship Some 3
Hyperostosis cranialis interna Clinical course True Progressive Inferred relationship Some 5
Progressive scapulohumeroperoneal distal myopathy Clinical course True Progressive Inferred relationship Some 2
Cerebellar ataxia with oculomotor apraxia type 4 Clinical course True Progressive Inferred relationship Some 1
PLAA-associated neurodevelopmental disorder Clinical course True Progressive Inferred relationship Some 2
Severe myopia, generalised joint laxity, short stature syndrome Clinical course True Progressive Inferred relationship Some 5
NKX6-2-related autosomal recessive hypomyelinating leucodystrophy Clinical course True Progressive Inferred relationship Some 4
Autosomal dominant mitochondrial myopathy with exercise intolerance Clinical course True Progressive Inferred relationship Some 1

Start Previous Page 5 of 7 Next End

Reference Sets

Qualifier value foundation reference set

Back to Start