Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Recurrent venous leg ulcer |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent candidiasis of vagina |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent renal disease following transplantation of kidney (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent ventricular tachycardia |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent proliferative glomerulonephritis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent primary malignant neoplasm of vulva (disorder) |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Chronic recurrent pilonidal cyst without abscess |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent deep vein thrombosis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent infective cystitis |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Noninfectious variant with a clinical presentation similar to that of the acute disease but with less coryza. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent croup |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent rectal polyp |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent cystitis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent squamous cell carcinoma (disorder) |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent malignant neoplasm of prostate (disorder) |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent primary malignant neoplasm of left female breast |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent primary malignant neoplasm of right female breast |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Frequent episodic tension-type headache (disorder) |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent ulcer of mouth (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
épilepsie partielle complexe récidivante |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent skin infection |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent cholesteatoma of mastoid cavity (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Right recurrent femoral hernia |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Left recurrent femoral hernia |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent vulvitis (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
A rare neurologic disease characterized by unpredictable, transient and spontaneous unresponsiveness lasting from hours to days, with a frequency of three to seven attacks per year, in the absence of readily discernible toxic, metabolic or structural causes. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Idiopathic recurrent pericarditis is a rare autoinflammatory syndrome defined as recurrence of pericardial inflammation of unknown origin following the first episode of acute pericarditis and a symptom-free interval of 4-6 weeks or longer. Recurrent attacks of chest pain may be the sole presentation or the chest pain may be accompanied by pericardial friction rub, electrocardiographic or echocardiographic changes, pericardial effusion and increased C-reactive protein. Cardiac tamponade is a rare, life-threatening complication. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent benign focal seizures of childhood |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Acute recurrent inflammation of salivary gland (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent ulcer of vulva caused by human herpes simplex virus |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent femoral hernia (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent inflammation of vulva caused by human herpes simplex virus (disorder) |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Palindromic rheumatism |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent kidney stone |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent respiratory papillomatosis (disorder) |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent bronchiectasis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent cholangitis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Superior limbic keratoconjunctivitis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent cyst of breast |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Disseminate infundibulo-folliculitis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent melanocytic nevus (disorder) |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Behcet's syndrome |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Generalized pustular psoriasis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Chronic recurrent pilonidal cyst (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Hereditary periodic fever (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent primary malignant neoplasm of vagina |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent ventricular septal defect following procedure (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent peritonsillar abscess |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent angina status post coronary artery bypass graft (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent angina status post directional coronary atherectomy (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent angina status post percutaneous transluminal coronary angioplasty (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent angina status post rotational atherectomy (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent angina following placement of coronary artery stent (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent infection due to specific granule deficiency |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent infection due to immunoglobulin isotype deficiency (disorder) |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
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. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome is a rare, genetic, neurodegenerative disease characterized by episodic metabolic encephalomyopathic crises (of variable frequency and severity which are frequently precipitated by an acute illness) which manifest with profound muscle weakness, ataxia, seizures, cardiac arrhythmias, rhabdomyolysis with myoglobinuria, elevated plasma creatine kinase, hypoglycemia, lactic acidosis, increased acylcarnitines and a disorientated or comatose state. Global developmental delay, intellectual disability and cortical, pyramidal and cerebellar signs develop with subsequent progressive neurodegeneration causing loss of expressive language and varying degrees of cerebral atrophy. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
A rare genetic hematologic and intestinal disease characterized by childhood onset of bleeding tendency with epistaxis, gum bleeding, gastrointestinal bleeding, hematuria, and menorrhagia due to impaired platelet aggregation and secretion, as well as recurrent gastrointestinal ulcer. Mildly reduced levels of coagulation factor XI have been reported in addition. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
A rare genetic immune disease characterized by recurrent sinopulmonary infections and autoimmune enterocolopathy, manifesting as frequent episodes of intractable diarrhea with abdominal pain and fever, accompanied by eczematous rashes, due to deficits in components of innate and adaptive immunity. Immunologic abnormalities include IgG subclass deficiency, impaired antigen-induced lymphocyte proliferation, reduced cytokine production by CD8+ T lymphocytes, and decreased numbers of natural killer cells. |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
A rare genetic immune disease characterized by early onset of recurrent bacterial, viral, and fungal infections, chronic inflammatory bowel disease, gastritis, and inflammatory polyarthritis. Patients present with diarrhea, vomiting, hepatosplenomegaly, mouth ulcers, perianal abscesses, chronic lung disease with bronchiectasis, and failure to thrive. Occurrence of a skin rash associated with lymphocytic vasculitis has also been reported. Immunologic abnormalities include variable T-cell lymphopenia, decreased natural killer cells, and decreased B-cells with variable hypogammaglobulinemia. |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
Hereditary paediatric Behçet-like disease |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent anterior uveitis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Chronic nonbacterial osteomyelitis (CNO), also known as chronic recurrent multifocal osteomyelitis (CRMO), is a chronic autoinflammatory syndrome that is characterised by multiple foci of painful swelling of bones, mainly in the metaphyses of the long bones, in addition to the pelvis, the shoulder girdle and the spine. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent salmonella sepsis co-occurrent with human immunodeficiency virus infection |
Is a |
False |
Recurrent disease |
Inferred relationship |
Some |
|
A rare genetic neurological disorder characterized by infantile or childhood onset of recurrent acute encephalopathic episodes with cerebellar and extrapyramidal involvement following febrile illnesses. During the episodes, patients typically show sudden onset of truncal ataxia, occasionally accompanied by lethargy and impairment of speech, as well as choreic and athetoid movements, seizures, loss of deep tendon reflexes, and presence of pathological reflexes. Episodes last from day to weeks and may leave residual symptoms such as speech impairment and poor coordination. There have been no further descriptions in the literature since 1983. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
A rare genetic parenchymatous liver disease characterized by infantile or early childhood onset of recurrent episodes of acute liver failure precipitated by a febrile illness. During the life-threatening episodes, patients present with vomiting, lethargy, jaundice, as well as elevated levels of liver enzymes and coagulopathy. There is usually complete recovery between the episodes with conservative treatment. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Stuttering priapism |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent isolated sleep paralysis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Relapsing febrile nodular nonsuppurative panniculitis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Ligneous conjunctivitis (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
A rare inflammatory optic neuropathy characterized by recurrent episodes of idiopathic inflammation of the optic nerve head with optic disc edema associated with macular exudate in a star-shaped pattern. Patients present with acute visual loss, most typically in the form of a large central scotoma. Pain is mild or absent. Bilateral involvement is frequent and usually sequential. The interval between attacks is highly variable, ranging from months to several years. Visual loss is cumulative with each attack and often severe. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent venous ulcer of lower limb |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent neoplasm (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent glomerulonephritis following transplantation of kidney (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent phimosis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Lipogranulomatosis subcutanea of Rothmann and Makai |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent infectious disease (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent aspiration pneumonitis |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
A rare ophthalmic disorder characterized by periodic inflammatory attacks of the cornea manifesting as unilateral ocular pain, conjunctival hyperemia, photophobia and epiphora lasting for 1 to 3 days, followed by blurred vision for several weeks. Caused by a heterozygous pathogenic variant c.61G>C, p.(Asp21His) in the NLRP3 gene. The pathogenic variant is highly penetrant (95%). The disease is autosomal dominant. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent obturator hernia (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent lumbar hernia (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent incisional hernia |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
A rare otorhinolaryngologic disease characterized by recurrent and severe obstruction of the central airway in the region bounded superiorly by a plane below the glottis and inferiorly by the first two tracheal rings. Symptoms may involve respiratory distress, dysphonia, exertional dyspnea, stridor, chronic cough and wheezing. Diagnosis is challenging due to the lack of apparent etiology and nonspecific respiratory symptoms that can be confounded with other common respiratory diseases and may also occur in late course of the disease. Thorough clinical and laboratory evaluation aims to exclude other causes of subglottic stenosis is therefore essential. Affected patients are almost exclusively Caucasian women between 30-60 years old. |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Acute recurrent allergic otitis media |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|
Recurrent transient cerebral ischemic attack (disorder) |
Is a |
True |
Recurrent disease |
Inferred relationship |
Some |
|