Disease Index
9,486 diseasesidiopathic chronic eosinophilic pneumonia
MeSH: C535590
idiopathic congenital hypothyroidism
Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism (see this term) whose cause and prevalence are unknown
idiopathic disseminated cytomegalovirus infection
human disease
idiopathic dropped head syndrome
human disease
idiopathic ductopenia
human disease
idiopathic eosinophilic myositis
human disease
MeSH: C535895
idiopathic eosinophilic pneumonia
human disease
idiopathic giant-cell myocarditis
human disease
ICD: I40.8
idiopathic hemiconvulsion-hemiplegia syndrome
human disease
idiopathic hydrops fetalis
Human disease
ICD: P83.2
idiopathic hypercalciuria
human disease
idiopathic hypersomnia
neurological disorder which is characterized primarily by excessive sleep and excessive daytime sleepiness
ICD: G47.12MeSH: D020177
idiopathic hypersomnia with long sleep time
idiopathic hypersomnia without long sleep time
Idiopathic inflammatory demyelinating disease
human disease
idiopathic inflammatory myopathy
idiopathic interstitial pneumonia
pneumonia located in the lung parenchyma of unknown cause
MeSH: D054988
idiopathic juvenile osteoporosis
osteoporosis with no known cause that is characterized by pain in the back and extremities, walking difficulties, multiple fractures, and radiological evidence of osteoporosis
MeSH: C537700
idiopathic linear interstitial keratitis
human disease
idiopathic localized lipodystrophy
idiopathic macular telangiectasia type 1
human disease
idiopathic macular telangiectasia type 3
human disease
idiopathic malabsorption due to bile acid synthesis defects
Idiopathic malabsorption due to increased acid bile synthesis is an intestinal disease of unknown etiology characterized by an overproduction of bile acids which leads to chronic watery diarrhea
idiopathic male infertility
human disease
idiopathic membranous glomerulonephritis
Idiopathic membranous glomerulonephritis (IMG) is a primary glomerular disease characterized by proteinuria, usually in the nephrotic range, with preserved renal function
idiopathic neonatal atrial flutter
idiopathic nephrotic syndrome
Nephrotic syndrome for which no cause has been identified
idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
human disease
idiopathic panuveitis
human disease
idiopathic peliosis hepatis
human disease