Trusted information across 10,888 rare diseases — plain language, always cited, free for everyone.
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Data syncs range from 3x daily (news) to weekly (trials, FDA). Reports regenerate when data changes.
Showing 9,141-9,160 of 10,888 diseases
MONDO:0014828
MONDO:0014829
MONDO:0979233
MONDO:0012291
Immunoglobulin A deficiency 2 is a condition characterized by a selective deficiency in immunoglobulin A, an important antibody in the immune system....
MONDO:0019167
Immunoglobulin A vasculitis is a systemic condition characterized by inflammation of small blood vessels. It primarily manifests with a distinctive sk...
MONDO:0017287
Immunoglobulin G4-related sclerosing disease is a condition characterized by mass-forming lesions that commonly affect the pancreas, submandibular and...
MONDO:0000583
Immunoglobulin beta deficiency is a condition that appears to impact the immune system, although detailed information on its biological underpinnings...
MONDO:0015697
MONDO:0850368
Immunoglobulin heavy-and-light chain amyloidosis is a condition in which abnormal deposits of amyloid fibrils, formed by fragments of immunoglobulin h...
MONDO:0014005
Immunoglobulin-mediated membranoproliferative glomerulonephritis is a kidney disorder marked by inflammation and immune complex deposition that leads...
MONDO:0044312
MONDO:0019991
MONDO:0019605
MONDO:0957423
MONDO:0001046
Imperforate anus is a congenital condition characterized by the absence of a normal anal opening, typically identified shortly after birth. It represe...
MONDO:0017162
MONDO:0017686
Inborn aminoacylase deficiency is an inherited metabolic disorder characterized by a disruption in aminoacylase activity. This condition is linked to...
MONDO:0019214
Inborn carbohydrate metabolic disorder is an inherited metabolic condition that arises from a disruption in the process of carbohydrate metabolism. Re...
MONDO:0019189
The inborn disorder of amino acid and other organic acid metabolism is a metabolic condition that can affect multiple organ systems. Although the prec...
MONDO:0004736
Inborn disorder of amino acid metabolism is an inherited condition that disrupts the normal processing of amino acids in the body. It encompasses a ra...
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