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281302008: Above reference range (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
419285019 Above reference range en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
674822016 Above reference range (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3824241000005112 over referenceinterval da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Above reference range (qualifier value) Is a Reference range comments false Inferred relationship Some
Above reference range (qualifier value) Is a Outside reference range (qualifier value) true Inferred relationship Some
Above reference range (qualifier value) Is a Increased true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Grain fever Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Metal fever Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Polymer fume fever Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Copper fever Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Spelters' fever (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Toxic inhalation-induced febrile illness Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Humidifier fever Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Pulmonary mycotoxicosis Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Febrile disorder (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Brass-founders' fever Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Familial febrile convulsions Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Acute febrile mucocutaneous lymph node syndrome Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Acute febrile neutrophilic dermatosis Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Sweet's disease following infection (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Febrile convulsion Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Recurrent febrile convulsion Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Sweet's disease caused by drug Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Simple febrile seizure (finding) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Complex febrile seizure (finding) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Febrile granulocytopenia (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Febrile leukopenia (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Severe fever with thrombocytopenia syndrome (SFTS) is a newly emerging infectious disease. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
A rare genetic familial partial epilepsy disease with characteristics of simple partial seizures, complex partial seizures and/or secondarily generalized seizures, originating from the inner aspect of the temporal lobe, associated with an antecedent history of febrile seizures, occurring in various members of a family. Hippocampal abnormalities (for example hippocampal sclerosis) may also be associated. There is evidence the disease is caused by homozygous mutation in the CPA6 gene on chromosome 8q13. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Febrile neutropenia (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Febrile urinary tract infection Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Familial Mediterranean fever Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Familial amyloid nephropathy with urticaria AND deafness Has interpretation True Above reference range (qualifier value) Inferred relationship Some 6
Familial cold urticaria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Chronic infantile neurological, cutaneous and articular syndrome Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Hereditary periodic fever (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Febrile ulceronecrotic pityriasis lichenoides acuta (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
TNF receptor-associated periodic fever syndrome (TRAPS) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
A rare autoinflammatory disease and form of mevalonate kinase deficiency (MKD), characterised by periodic attacks of fever and a systemic inflammatory reaction (cervical lymphadenopathy, abdominal pain, vomiting, diarrhoea, arthralgia and skin manifestations). The disease usually begins in the first year of life and rarely after 5 years of age. HIDS is an inherited syndrome caused by mutations in the mevalonate kinase (MVK) gene (12q24). These MVK mutations lead to reduced, but not abolished enzyme activity. This in turn leads to impaired control of the production of inflammatory mediators, which in turn cause inflammatory (fever) attacks. The disease follows an autosomal recessive pattern of inheritance. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Cryopyrin associated periodic syndrome (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
A rare hereditary immune deficiency with skin involvement characterized by early-onset cold urticaria after generalized exposure to cold air or evaporative cooling and not after contact with cold objects. Additional immunologic abnormalities are often present - antibody deficiency, recurrent infections, autoimmune disease and symptomatic allergic disease. Caused by heterozygous deletion within the PLCG2 gene on chromosome 16q23. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
A rare autoinflammatory syndrome with characteristics of episodic and recurrent periods of fever combined with various systemic manifestations such as myalgia, arthralgia, joint swelling, urticaria, headache and skin rash. Common trigger of these episodes is cold. There is evidence the disease is caused by heterozygous mutation in the NLRP12 gene on chromosome 19q13. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
A rare genetic autoinflammatory syndrome with immune deficiency characterized by a combination of autoinflammation, immunodeficiency, and neutrophil dysfunction, as well as mild bleeding diathesis. Patients present recurrent attacks of abdominal pain, high fever, and systemic inflammation lasting four to five days and occurring every few weeks. Attacks may be accompanied by nailbed, tongue, submandibular, and gluteal abscesses, intra-abdominal granulomas, pyoderma gangrenosum, and buccal ulcerations. Frequent episodes of purulent paronychia, superficial skin and mucosal infections, and purulent upper respiratory tract infections have also been reported. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
A rare anomaly of puberty or/and menstrual cycle characterized by recurrent fevers (higher than 38 degrees Celsius) associated with the luteal phase of the menstrual cycle in women. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Myoclonus associated with fever Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
PFAPA (Periodic fever - aphthous stomatitis- pharyngitis - adenopathy) syndrome is an auto inflammatory syndrome characterized by recurrent febrile episodes associated with aphthous stomatitis, pharyngitis and cervical adenitis. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 5
Macrophage activation syndrome due to juvenile systemic onset arthritis Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Melorheostosis with osteopoikilosis is a rare sclerosing bone dysplasia, combining the clinical and radiological features of melorheostosis and osteopoikilosis, that has been reported in some families with osteopoikilosis and that is characterized by a variable presentation of limb pain and deformities. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
A rare, endocrine disease characterized by early onset of polycythemia, and later occurring multiple paraganglioma. Clinical presentation includes hypertension, headaches, fatigue, nausea, anxiety, and high concentration of red blood cells, leading to increased risk of stroke and pulmonary thromboembolism. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
A rare genetic hyperlipidemia characterized by excessive increase in plasma triglyceride levels due to the accumulation of chylomicrons, which manifests biochemically as severe hypertriglyceridemia. Clinical manifestations include recurrent episodes of acute pancreatitis, abdominal pain, nausea, fatigue, diarrhea, hepatosplenomegaly, eruptive xanthomas, lipemia retinalis and failure to thrive. Children may be asymptomatic with later onset of symptoms. The condition is not associated with severe atherosclerosis. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Hyperlipoproteinemia, type I Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Hyperthermia (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
A rare genetic systemic or rheumatologic disease characterized by neonatal or infantile onset of enterocolitis (which resolves with age), periodic fever, and episodes of severe systemic inflammation, which may be precipitated by infections, stress, or fatigue. Signs and symptoms include splenomegaly, urticaria-like rashes, arthralgia, and myalgia. Associated laboratory findings are elevated inflammatory markers (such as ferritin, C-reactive protein), pancytopenia, and elevated transaminases. If left untreated, flares can progress to coagulopathy, organ failure, and death. Has interpretation True Above reference range (qualifier value) Inferred relationship Some 6
Nephrogenous proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Essential proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Pyogenic proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Prerenal proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Emulsion proteinuria (finding) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Residual proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Adventitious proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
True proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Enterogenic proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Functional proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Hematogenous proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Febrile proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Cardiac proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Globular proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Postrenal proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Lordotic proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Colliquative proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Overflow proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Palpatory proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Gouty proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Acute nephritic syndrome, diffuse crescentic glomerulonephritis Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Chronic nephritic syndrome Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Chronic nephritic syndrome, minor glomerular abnormality Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
isoleret proteinuri med specificeret morfologisk læsion Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
isoleret proteinuri med specificeret morfologisk forandring, mindre glomerulær abnormitet Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
isoleret proteinuri med specificeret morfologisk forandring, fokale og segmentære glomerulære morfologiske forandringer Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
isoleret proteinuri med specificeret morfologisk forandring, diffus membranøs glomerulonefrit Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
isoleret proteinuri med specificeret morfologisk forandring, diffus mesangial proliferativ glomerulonefrit Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
isoleret proteinuri med specificeret morfologisk forandring, diffus endokapillær proliferativ glomerulonefrit Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
isoleret proteinuri med specificeret morfologisk forandring, diffus membranoproliferativ glomerulonefrit Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
isoleret proteinuri med specificeret morfologisk forandring, dense deposit disease Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
isoleret proteinuri med specificeret morfologisk forandring, diffus koncentrisk glomerulonefrit Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
Nephrotic range proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Proteinuria of adolescence Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
fordøjelsesproteinuri Has interpretation False Above reference range (qualifier value) Inferred relationship Some 1
Dietetic proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Microalbuminuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Protein-losing nephropathy (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Exercise proteinuria Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Recurrent proteinuria (finding) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 2
Nephritic syndrome Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Isolated proteinuria (finding) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 1
Persistent proteinuria (finding) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Macroalbuminuric nephropathy due to diabetes mellitus (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3
Chronic nephritic syndrome with membranous glomerulonephritis Has interpretation True Above reference range (qualifier value) Inferred relationship Some 5
Proteinuria due to type 2 diabetes mellitus Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Chronic nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III Has interpretation True Above reference range (qualifier value) Inferred relationship Some 5
Isolated proteinuria co-occurrent and due to membranoproliferative glomerulonephritis type III Has interpretation False Above reference range (qualifier value) Inferred relationship Some 4
Nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III Has interpretation True Above reference range (qualifier value) Inferred relationship Some 5
Proteinuric nephropathy due to diabetes mellitus (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Persistent proteinuria due to type 2 diabetes mellitus (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 5
Proteinuria due to type 1 diabetes mellitus (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 4
Persistent proteinuria due to type 1 diabetes mellitus (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 5
Melorheostosis of spine (disorder) Has interpretation True Above reference range (qualifier value) Inferred relationship Some 3

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