Disease Directory

IVIC syndrome is a very rare genetic condition that affects several parts of the body. It is characterized by differences in the upper limbs, such as...

IgA glomerulonephritis is a kidney condition where a specific part of the kidney’s filtering units, called glomeruli, become inflamed. This inflammati...

Information about overview is currently limited for this condition.

IgAD1 is a condition in which people have very low or absent levels of immunoglobulin A (IgA) in the blood, while levels of immunoglobulin G and immun...

Information about overview is currently limited for this condition.

IgG4-related dacryoadenitis and sialoadenitis, also known historically as Mikulicz disease, is a condition marked by persistent, usually painless enla...

Information about overview is currently limited for this condition.

IgG4-related mediastinitis, also known as fibrosing mediastinitis, mediastinal fibrosis, sclerosing mediastinitis, or idiopathic mediastinal fibrosis,...

IgG4-related mesenteritis, also known as sclerosing mesenteritis, is a rare condition that causes inflammation in the fat tissue of the small bowel me...

IgG4-related ophthalmic disorder is a condition where the IgG4-related disease affects the eye. This condition involves an inflammatory process that i...

IgG4-related pachymeningitis, also known as idiopathic hypertrophic pachymeningitis, is a rare condition in which the dura, the outer layer of the bra...

IgG4-related retroperitoneal fibrosis, also known as Ormond disease or idiopathic retroperitoneal fibrosis, is a rare condition where a fibrous mass f...

Information about overview is currently limited for this condition.

IgG4-related submandibular gland disease is a chronic condition that affects the salivary glands. It is marked by a long-lasting fibrotic inflammatory...

IgG4-related thyroid disease, also known as Riedel thyroiditis, is a fibroinflammatory condition that affects the thyroid gland. In people with this c...

Iida Kannari syndrome is a rare disease. Detailed information about this condition is currently limited in medical literature.

Information about the overview is currently limited for this condition.

Imerslund-Grasbeck syndrome is a rare condition that affects the body’s ability to absorb vitamin B12. This syndrome is inherited in an autosomal rece...

Imerslund-Grasbeck syndrome type 1 is a rare genetic disorder that typically appears in infancy or early childhood. It is mainly characterized by mega...

Imerslund-Grasbeck syndrome type 2 is an autosomal recessive disorder that affects the body’s ability to absorb vitamin B12. This can lead to megalobl...