Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Grain fever |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Metal fever |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Polymer fume fever |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Copper fever |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Spelters' fever |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Toxic inhalation-induced febrile illness |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Humidifier fever |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Pulmonary mycotoxicosis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Febrile disorder (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Brass-founders' fever |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Familial febrile convulsions |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Acute febrile mucocutaneous lymph node syndrome (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Acute febrile neutrophilic dermatosis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Sweet's disease following infection (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Febrile convulsion |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Recurrent febrile convulsion |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Sweet's disease caused by drug |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Simple febrile seizure (finding) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Complex febrile seizure (finding) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Febrile granulocytopenia (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Febrile leukopenia (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Severe fever with thrombocytopenia syndrome (SFTS) is a newly emerging infectious disease. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
A rare, genetic, familial partial epilepsy disease characterized by 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 (e.g. hippocampal sclerosis) may also be associated. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Febrile neutropenia (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Febrile urinary tract infection |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Familial Mediterranean fever |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Familial amyloid nephropathy with urticaria AND deafness |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
6 |
Familial cold urticaria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Chronic infantile neurological, cutaneous and articular syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Hereditary periodic fever (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Febrile ulceronecrotic pityriasis lichenoides acuta (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
TNF receptor-associated periodic fever syndrome (TRAPS) |
Has interpretation |
True |
Above reference range |
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 |
Inferred relationship |
Some |
3 |
Cryopyrin associated periodic syndrome (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
A rare, hereditary, immune deficiency with skin involvement characterised by early-onset cold urticaria after generalised 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. |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
A rare autoinflammatory syndrome characterized by 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. |
Has interpretation |
True |
Above reference range |
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 |
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 |
Inferred relationship |
Some |
2 |
Myoclonus associated with fever |
Has interpretation |
True |
Above reference range |
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 |
Inferred relationship |
Some |
5 |
Macrophage activation syndrome due to juvenile systemic onset arthritis |
Has interpretation |
True |
Above reference range |
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 |
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 |
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 |
Inferred relationship |
Some |
1 |
Hyperlipoproteinemia, type I |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Hyperthermia (disorder) |
Has interpretation |
True |
Above reference range |
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 |
Inferred relationship |
Some |
6 |
Nephrogenous proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Essential proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Pyogenic proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Prerenal proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Emulsion proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Residual proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Adventitious proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
True proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Enterogenic proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Functional proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Hematogenous proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Febrile proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Cardiac proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Globular proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Postrenal proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Lordotic proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Colliquative proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Overflow proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Palpatory proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Gouty proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Acute nephritic syndrome, diffuse crescentic glomerulonephritis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Chronic nephritic syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Chronic nephritic syndrome, minor glomerular abnormality |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Isolated proteinuria with specified morphological lesion |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Isolated proteinuria with specified morphological lesion, minor glomerular abnormality |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Isolated proteinuria with specified morphological lesion, focal and segmental glomerular lesions |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Isolated proteinuria with specified morphological lesion, diffuse membranous glomerulonephritis |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Isolated proteinuria with specified morphological lesion, diffuse mesangial proliferative glomerulonephritis |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Isolated proteinuria with specified morphological lesion, diffuse endocapillary proliferative glomerulonephritis |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Isolated proteinuria with specified morphological lesion, diffuse mesangiocapillary glomerulonephritis |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Isolated proteinuria with specified morphological lesion, dense deposit disease |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Isolated proteinuria with specified morphological lesion, diffuse concentric glomerulonephritis |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Nephrotic range proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Proteinuria of adolescence |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Digestive proteinuria |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
1 |
Dietetic proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Microalbuminuria (finding) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Protein-losing nephropathy (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Exercise proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Recurrent proteinuria |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
2 |
Nephritic syndrome |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Isolated proteinuria (finding) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
1 |
Persistent proteinuria (finding) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Macroalbuminuric nephropathy due to diabetes mellitus (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |
Chronic nephritic syndrome with membranous glomerulonephritis |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
5 |
Proteinuria due to type 2 diabetes mellitus |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Chronic nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
5 |
Isolated proteinuria co-occurrent and due to membranoproliferative glomerulonephritis type III |
Has interpretation |
False |
Above reference range |
Inferred relationship |
Some |
4 |
Nephritic syndrome co-occurrent and due to membranoproliferative glomerulonephritis type III |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
5 |
Proteinuric nephropathy due to diabetes mellitus (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Persistent proteinuria due to type 2 diabetes mellitus (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
5 |
Proteinuria due to type 1 diabetes mellitus (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
4 |
Persistent proteinuria due to type 1 diabetes mellitus (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
5 |
Melorheostosis of spine (disorder) |
Has interpretation |
True |
Above reference range |
Inferred relationship |
Some |
3 |