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56,125 results found
You searched for “X” in All. RX Search found 56,125 result(s) and checks doctor-selected, exact-title, synonym, and related matches.
Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency or Bangstad syndrome is a very rare inherited condition. Children are unusually small before...
Late-onset multiple carboxylase deficiency is a rare, inherited problem of biotin (vitamin B7) use and recycling. Biotin is a helper for several enzymes called carboxylases. These...
Juvenile-onset multiple carboxylase deficiency (MCD) is an umbrella term for problems in the body’s biotin system. Biotin is a vitamin (vitamin B7) that helps important enzymes,...
Maxillonasal dysplasia syndrome—often called Binder syndrome—is a rare condition present at birth. It mainly affects the middle of the face, especially the upper jaw (premaxilla) and...
Maxillonasal dysostosis is a rare, birth-present (congenital) condition in which the middle of the face and the nose are under-developed. The bridge of the nose looks...
Binder type maxillonasal dysplasia—often called Binder syndrome—is a rare condition present at birth in which the central face does not develop fully, especially the upper jaw...
Maxillo-nasal dysplasia (often called Binder syndrome) is a rare birth condition where the middle part of the face—especially the upper jaw (premaxilla) and the nose—does not...
Complex cortical dysplasia with other brain malformations 14A, often shortened to CDCBM14A, is a rare, inherited brain-development disorder. Before birth, the outer layer of the brain...
Hypogonadism-short stature-coloboma-preaxial polydactyly syndrome is a very rare, inherited condition reported only in a small number of people. It affects several body systems at once. The...
Thrombocytopenia with X-linked recessive beta-thalassemia is a rare, inherited blood disorder that affects two blood cell lines at the same time: platelets (which help stop bleeding)...
Beta-thalassemia–X-linked thrombocytopenia syndrome is a rare, inherited blood disorder that mainly affects boys and men. It happens when a gene on the X chromosome called GATA1...
Peroxisomal thiolase deficiency (historical label) was used for a suspected single-enzyme defect of the peroxisome pathway (enzyme: peroxisomal 3-ketoacyl-CoA thiolase, gene ACAA1). Later work re-examined the...
