Disease Index
9,486 diseasesidiopathic phalangeal acro-osteolysis
human disease
idiopathic posterior uveitis
human disease
idiopathic pulmonary arterial hypertension
idiopathic pulmonary artery dilatation
idiopathic pulmonary fibrosis
chronic, irreversible and ultimately fatal disease characterized by a progressive decline in lung function
MeSH: D054990
idiopathic recurrent and disabling cutaneous herpes
human disease
idiopathic recurrent pericarditis
human disease
idiopathic recurrent stupor
Idiopathic sclerosing mesenteritis
medical condition
idiopathic severe pneumococcemia
human disease
idiopathic spontaneous coronary artery dissection
human disease
MeSH: C565153
idiopathic steroid-sensitive nephrotic syndrome
Steroid-sensitive nephrotic syndrome (SSNS) is a kidney disease defined by selective proteinuria, hypoalbuminaemia and, on renal biopsy, minimal changes without immunoglobulin deposits
idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation
human disease
idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis
human disease
idiopathic steroid-sensitive nephrotic syndrome with minimal change
human disease
idiopathic syringomyelia
idiopathic uveal effusion syndrome
rare eye disease
MeSH: D000080323
idiopathic ventricular fibrillation, non Brugada type
human disease
IGAN2
human disease
IgG4-related aortitis
human disease
IgG4-related disease
systemic fibroinflammatory disease, associated with elevated serum IgG4 levels in about 70% of cases
MeSH: D000077733
IgG4-related hepatopathy
Inflammatory pseudotumor (IPT) of the liver is a rare benign tumor-like lesion
IgG4-related kidney disease
human disease
IgG4-related ophthalmic disease
human disease
IgG4-related pachymeningitis
human disease
IgG4-related sclerosing cholangitis
human disease
IgG4-related submandibular gland disease
human disease
IGSF1 deficiency syndrome
X-linked disease characterized by hypothyroidism that is present at birth, delayed testosterone increase in puberty, and testicular enlargement in adulthood that has material basis in mutation of the IGSF1 gene on chromosome Xq26
Il-1R–Associated kinase 4 deficiency
Interleukin-1 receptor-associated kinase-4 (IRAK-4) deficiency is an immunodeficiency associated with increased susceptibility to invasive infections caused by pyogenic bacteria
MeSH: C564352
ileal neuroendocrine tumor, well differentiated, low or intermediate grade
well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the ileum