Malignant Mixed Mesodermal (Müllerian) Tumor (MMMT)
Malignant mixed mesodermal (Müllerian) tumor (MMMT)—now usually called uterine carcinosarcoma—is a rare, fast-growing cancer that starts in the lining of the uterus (the endometrium). It is...
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Malignant mixed mesodermal (Müllerian) tumor (MMMT)—now usually called uterine carcinosarcoma—is a rare, fast-growing cancer that starts in the lining of the uterus (the endometrium). It is...
Excessive serotonin secretion means the body has too much serotonin in the wrong place or at the wrong time. Serotonin is a natural chemical that helps...
Chronic Ataxic Neuropathy, Ophthalmoplegia, Monoclonal Immunoglobulin M Protein, Cold Agglutinin and Disialosyl Antibody Syndrome is a rare, long-lasting, immune-mediated nerve disease. The immune system makes a...
Chronic ataxic neuropathy-ophthalmoplegia-IgM paraprotein-cold agglutinins-disialosyl antibodies syndrome is a rare, long-lasting autoimmune nerve disease. Your immune system makes a monoclonal IgM antibody that wrongly targets disialosyl...
CANOMAD is a rare, chronic, immune-mediated nerve disorder. The full name summarizes its key features: Chronic Ataxic Neuropathy with Ophthalmoplegia (eye-movement weakness), an IgM monoclonal M-protein...
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis (CACP) syndrome is a rare genetic condition that begins in childhood and combines four main problems: bent fingers that won’t fully straighten (camptodactyly), large-joint...
Spinocerebellar Ataxia, Autosomal Recessive 5 is a very rare, inherited brain disorder that mainly damages the cerebellum (the balance and coordination center). It is caused by...
Cerebellar ataxia-intellectual disability-optic atrophy-skin abnormalities syndrome is a rare, inherited brain-development disorder. Children are born with poor balance and coordination (congenital cerebellar ataxia) that stays non-progressive...
Calciphylaxis is a rare but very serious disease of small blood vessels in the skin and fat. Calcium builds up in the walls of tiny arterioles....
Contiguous ABCD1–DXS1357E deletion syndrome (CADDS) is a very rare X-linked genetic condition in which a small piece of the X chromosome is missing at the band...
Flax-dressers’ disease is a breathing problem caused by regularly inhaling flax plant dust while preparing or processing flax fibers. The very small dust pieces—and the bacterial...
X-Linked Recessive Agammaglobulinemia is a rare genetic condition that mainly affects boys and stops the body from making antibodies. Antibodies are proteins that help you fight...