Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Chronic idiopathic monocytosis |
Has definitional manifestation |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic anaphylaxis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic gynecomastia (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic rapidly progressive glomerulonephritis (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
purpura thrombopénique idiopathique |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic exfoliative cheilitis (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic eosinophilic pneumonitis (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic atrophoderma of Pasini and Pierini |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic neonatal atrial flutter (AFL) is a rare rhythm disorder, characterized by sustained tachycardia in newborns and infants with an atrial rate often at around 440 beats/minute (range 340-580). AFL may manifest as asymptomatic tachycardia, congestive heart failure or hydrops. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
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. |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
A rare congenital heart malformation of unknown etiology that is characterized by an extremely dilated right atrium, and that is usually asymptomatic and fortuitously discovered by echocardiography or chest radiography, and can be sometimes associated with other anomalies such as atrial arrhythmias (e.g. atrial flutter, atrial fibrillation, supraventricular tachycardia), severe tricuspid regurgitation, or atrial thrombus that could lead to potentially life-threatening thromboembolic complications. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Sporadic idiopathic steroid-resistant nephrotic syndrome (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic congenital hypothyroidism (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic megaesophagus (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic glomerular disease (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic premature ovarian failure (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic short stature (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Obscure gastrointestinal hemorrhage (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic portal hypertension (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic granulomatous hepatitis (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic pure sudomotor failure (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic aseptic osteonecrosis |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic syringomyelia (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Sudden idiopathic hearing loss (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
A rare non-hereditary degenerative ataxia disease characterized by a slowly progressive cerebellar syndrome (with ataxia of stance and gait, upper limb dysmetria and intention tremor, ataxic speech, and oculomotor abnormalities), presenting in adulthood (at around 50 years of age), that is not due to a known cause. Extracerebellar symptoms (e.g., decreased vibration sense and absent or decreased ankle reflexes), polyneuropathy and mild autonomic dysfunction may also be present. Mild cognitive impairment has also rarely been reported. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Chronic idiopathic pain syndrome (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic bilateral vestibulopathy is a rare otorhinolaryngologic disease characterized by dysfunction of both peripheral labyrinths or of the eighth cranial nerves, which presents with persistent unsteadiness of gait (particularly in darkness, during eye closure or under impaired visual conditions, or when standing/walking on uneven, soft or wobbly ground) and oscillopsia associated with head movements. The disease may be progressive, presenting no episodes of vertigo, or sequential, presenting recurrent episodes of vertigo. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Chronic idiopathic monocytosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
A rare, brain inflammatory disease characterized by thickening of the dura mater of the cranium or spine with at least two histopathological features of IgG4-related disease: dense lymphoplasmacytic infiltrate, storiform fibrosis, and/or obliterative phlebitis. Patients typically have non-specific CSF findings and might be without systemic involvement or serum IgG4 elevation. Clinical manifestations are caused by mechanical compression of nerve or vascular structure, leading to functional deficit, most commonly headache, cranial nerve palsies, vision problems and motor weakness. |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Chronic left idiopathic vestibulopathy |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Chronic right idiopathic vestibulopathy (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic CD4 lymphocytopenia is a rare primary immunodeficiency disorder characterized by persistent CD4 T-cell lymphopenia (less than 300 cells/µL on multiple occasions) not associated with any other underlying primary or secondary immune deficiency. Patients typically present opportunistic infections (with cryptococcal, mycobacterial, candidal, varicella zoster virus infections and progressive multifocal leukoencephalopathy being the most prevalent), malignancies (mainly lymphoproliferative disorders), or autoimmune disorders. Some individuals are asymptomatic and incidentally diagnosed. |
Is a |
True |
Idiopathic 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 |
Idiopathic disease |
Inferred relationship |
Some |
|
Chronic idiopathic constipation |
Is a |
True |
Idiopathic 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 |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic panuveitis is a rare inflammatory eye disease, of unknown etiology, characterized by generalized inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic, unilateral or bilateral visual impairment and ocular discomfort or pain. Patients present an increased risk of development of cataracts, secondary glaucoma, cystoid macular edema and/or retinal detachment. It could potentially result in vision loss. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic bronchiectasis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic osteoporosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic edema |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
A rare, idiopathic skin disease characterized by widespread, congenital, superficial erosions and vesicles (often involving more than 75% of the body) which heal leaving scars with a supple, symmetrical, reticulated pattern, frequently resulting in cicatricial alopecia and hyperthermia and/or hypohidrosis. Nail anomalies, neurodevelopmental and ophthalmologic abnormalities, tongue atrophy and preterm birth, with or without history of chorioamnionitis, are commonly associated. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic juxtafoveal telangiectasia (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic linear interstitial keratitis is a rare, acquired ocular disease characterized by migratory or non-migratory, horizontal, linear, stromal infiltrates that may heal spontaneously. Minimal vascularization and scarring may be observed but vision loss is not associated. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic posterior uveitis is a rare, potentially sight-threatening, ocular disease, not attributed to any specific ocular or systemic cause, characterized by focal, multifocal or diffuse non-infectious inflammation in the posterior uvea (i.e. choroiditis, chorioretinitis, retinitis and neuroretinitis). Visual morbidity due to complications (including cystoid macular edema and choroidal neovascularization) has been reported. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
A rare idiopathic inflammatory myopathy characterized by eosinophilic infiltration and inflammatory lesions of the skeletal muscle tissue, in the absence of an identifiable causative factor (e.g. parasitic infection, drug intake, systemic or malignant disease). Clinically patients may present focal or generalized muscle weakness and pain, difficulties to walk, motor clumsiness and/or mild bilateral Achilles tendon contracture, as well as elevated serum creatine kinase levels and peripheral blood and/or bone marrow hypereosinophilia. |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
A rare panuveitis characterized by uni- or bilateral abnormal fluid accumulation within the suprachoroidal space, resulting in internal choroidal elevation, in the absence of any known cause, such as decreased intraocular tension, intraocular tumor, intraocular inflammation or nanophthalmos. Patients typically present a protracted, relapsing-remitting course of visual acuity loss and fundus examination shows annular celio-choroidal detachment and shifting, serous retinal detachment. |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic granulomatous interstitial nephropathy |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
A rare retinal vasculopathy disease characterized by idiopathic retinal vasculitis (IRV), aneurysmal dilations (A) at arteriolar bifurcations, and neuroretinitis (N), which if untreated progresses to peripheral capillary non-perfusion, retinal neovascularization, and macular exudation, leading to severe, bilateral vision loss. |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic osteolyses |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic polyarthritis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic acute tubulointerstitial nephritis (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic interstitial pneumonitis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic capillaritis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic inflammatory myopathy (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
A rare neurological disease characterized by a generally deep, poorly localized, persistent facial pain that does not present characteristics of a cranial neuralgia and which cannot be attributed to another disorder. |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic scoliosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic hair dystrophy |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic calcification of skin |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic interstitial tubulonephritis (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic hypersomnia (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic pulmonary arteriosclerosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic chronic tubulointerstitial nephritis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic diffuse pulmonary ossification |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic pulmonary hemosiderosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic atrophic hypothyroidism |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic mid-dermal elastolysis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic hypereosinophilic syndrome (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic hepatitis in infancy |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Localized idiopathic lipoatrophy |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic guttate hypomelanosis |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic central precocious puberty |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic hydronephrosis (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic non-arteritic posterior ischemic optic neuropathy (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
neuropathie optique ischémique non artéritique idiopathique |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Leber idiopathic stellate neuroretinitis |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
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. |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic fold of choroid of eye |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Primary idiopathic hypertrophic cardiomyopathy |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Chronic idiopathic thrombocytopenic purpura (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
purpura thrombopénique aigu idiopathique |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic hilar fibrosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic cyst of iris |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic peripheral neuropathy |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic adductor spastic dysphonia |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic gingival fibromatosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic hypochromic anaemia |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic chronic pancreatitis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Congenital familial idiopathic priapism |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic ventricular fibrillation not Brugada type (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Disseminated idiopathic skeletal hyperostosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic livedo reticularis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic polypoidal choroidal vasculopathy |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic choroidal neovascular membrane (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic junctional ectopic tachycardia (disorder) |
Is a |
False |
Idiopathic disease |
Inferred relationship |
Some |
|
Chronic idiopathic immunoneutropenia in adult (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic megacolon |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Chronic idiopathic anhidrosis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic torsion dystonia (disorder) |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic hypercalcaemia |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Idiopathic acute pancreatitis |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|
Familial idiopathic hypercalciuria |
Is a |
True |
Idiopathic disease |
Inferred relationship |
Some |
|