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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
380497019 Progressive en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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
138851000077114 progressif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
138851000077114 progressif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Progressive Is a Chronic (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Acquired progressive lymphangioma (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Progressive angina (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Acquired progressive kinking of hair Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Cirrhosis of liver due to chronic hepatitis C (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Intrahepatic phlebosclerosis and fibrosis Clinical course False Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Hepatic fibrosis with hepatic sclerosis Clinical course False Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Cirrhosis of liver co-occurrent and due to primary sclerosing cholangitis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 5
Capsular portal cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Fatty portal cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Posthepatitic cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Micronodular cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cardiac cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Unilobular portal cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Syphilitic cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Parasitic cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Mixed micro and macronodular cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 5
Idiopathic copper-associated cirrhosis is a rare copper-overload liver disease characterized by a rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency and harboring a specific pathological aspect: pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 6
Glissonian cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Nutritional cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Cirrhosis of liver caused by methotrexate Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cirrhosis secondary to cholestasis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Infectious cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Juvenile portal cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Early cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Cryptogenic cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Florid cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Cirrhosis resulting from accumulation of iron in the liver. Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Macronodular cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Toxic cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Cirrhosis - non-alcoholic Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Cirrhosis of liver caused by methyldopa (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Drug-induced cirrhosis of liver Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cirrhosis of liver caused by amiodarone Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Advanced cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Primary biliary cholangitis Clinical course False Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cholangiolitic cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
PEHO-like syndrome is a rare, genetic neurological disease characterised by progressive encephalopathy, early-onset seizures with a hypsarrhythmic pattern, facial and limb oedema, severe hypotonia, early arrest of psychomotor development and craniofacial dysmorphism (evolving microcephaly, narrow forehead, short nose, prominent auricles, open mouth, micrognathia), in the absence of neuro-ophthalmic or neuroradiologic findings. Poor visual responsiveness, growth failure and tapering fingers are also associated. Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Portal cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Syphilitic portal cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Toxic portal cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Pigmentary portal cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Postnecrotic cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cruveilhier-Baumgarten syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Diffuse nodular cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Multilobular portal cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Secondary biliary cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Indian childhood cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Clonorchiasis with biliary cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cirrhosis and chronic liver disease Clinical course False Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Hepatic sclerosis Clinical course False Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Cirrhosis of liver due to hepatitis B Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Hypoxia-associated cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Laennec's cirrhosis, non-alcoholic Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Decompensated cirrhosis of liver (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Distal hereditary motor neuropathy type 1 (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1
Reynolds syndrome (RS) is an autoimmune disorder characterised by the association of primary biliary cirrhosis (PBC) with limited cutaneous systemic sclerosis (lcSSc). Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cardiac portal cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Latent cirrhosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Obstructive biliary cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cirrhotic cardiomyopathy Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 5
Biliary cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Alcoholic cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Biliary cirrhosis of children Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Bacterial portal cirrhosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Cirrhosis of liver (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Occult macular dystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculopharyngodistal myopathy (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1
Myoclonic epilepsy with ragged red fibers (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Huntington disease-like 3 Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1
Distal hereditary motor neuropathy type 7 (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary motor and sensory neuropathy type 5 (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary motor and sensory neuropathy with acrodystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1
Progressive polyneuropathy with bilateral striatal necrosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Charcot-Marie-Tooth disease type 2B5 (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary progressive mucinous histiocytosis Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive lower motor neuron disease with childhood onset Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Young adult-onset distal hereditary motor neuropathy Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant Charcot-Marie-Tooth disease type 2Q (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe neurodegenerative syndrome with lipodystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Childhood-onset spasticity with hyperglycinemia (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare genetic metabolite absorption and transport disorder characterised by progressive rod-cone dystrophy, usually presenting with impaired night vision in childhood, progressive loss of visual acuity and severe retinol deficiency without keratomalacia. Association with ocular colobomas, severe acne and hypercholesterolaemia has been reported. There is evidence the disease can be caused by homozygous or compound heterozygous mutation in the RBP4 gene chromosome 10q23. Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hypertrophy. Typically neck rigidity, rigid spine, Achilles tendon shortening and respiratory insufficiency later in disease course are present. The phenotype is caused by mutation in the FHL1 gene. Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Fatal post-viral neurodegenerative disorder Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 4
Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Mills syndrome (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperphosphatasemia tarda Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 5
A rare primary bone dysplasia characterized by the association of multiple epiphyseal dysplasia with macrocephaly and dysmorphic facial features (such as frontal bossing, hypertelorism, flat malar region, low-set ears, and short neck). Patients are of normal stature and present with joint swelling and genu valgum. Additional reported manifestations include clinodactyly, spindle-shaped fingers, and pectus excavatum. Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Pyknodysostosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Osteopetrosis - delayed type Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare congenital disorder of bone resorption characterised by generalised skeletal densification. Bone marrow failure, fractures and visual impairment are the classical features of the disease, which begins in early infancy or in fetal life. It results from the failure of osteoclasts to resorb immature bone. This leads to abnormal bone marrow cavity formation and to the clinical signs and symptoms of bone marrow failure. It is accompanied by hepatosplenomegaly due to compensatory extramedullary hematopoiesis. The disease is heterogeneous. Over 50% of cases are due to mutations in the TCIRG1 gene and another 10% are due to mutations in the CLCN7 gene. A small number of patients have been described with mutations in the OSTM1 gene. Transmission is autosomal recessive. Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 3
Sclerosteosis (disorder) Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 2
Muscle eye brain disease with bilateral multicystic leukodystrophy Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 6
A rare genetic neurological disorder characterised by early-onset progressive ataxia associated with myoclonic seizures (frequently associated with other seizure types such as generalised tonic-clonic, absence and drop attacks), scoliosis of variable severity, areflexia, elevated creatine kinase serum levels and relative preservation of cognitive function until late in the disease course. There is evidence the disease is caused by homozygous mutation in the GOSR2 gene on chromosome 17q21. Clinical course True Progressive Inferred relationship Existential restriction modifier (core metadata concept) 1

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