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 |