Browse medical articles by letter, category, and search. Built for large health libraries.
Before reading RX Patient Tools Use these quick guides before reading the article, or return to them when you need help preparing questions for a doctor....
DefinitionX-Linked Agammaglobulinemia (XLA), also known as Bruton’s agammaglobulinemia, is a rare genetic disorder that affects the immune system. In this article, we will explain XLA in...
DefinitionX-linked Angelman-like syndrome is a very rare brain and nerve (neurologic) condition that mostly affects boys. It happens when there is a change (mutation) in a...
DefinitionX-Linked Cardioskeletal Myopathy and Neutropenia?, often abbreviated as XL-CNM, is a rare genetic disorder that affects multiple systems in the body, including the heart, muscles, and...
DefinitionX-linked cardioskeletal myopathy and neutropenia? is a rare, inherited disease that mainly affects boys. It harms the heart muscle (cardiomyopathy), skeletal muscles (weakness? and low tone),...
DefinitionX-linked Charcot–Marie–Tooth disease (often abbreviated CMTX) is a hereditary peripheral neuropathy? that affects the insulating sheath (myelin) and the long fibers (axons) of nerves. It belongs...
DefinitionX-linked complicated corpus callosum dysgenesis is a rare genetic condition that affects the way the corpus callosum—the wide band of nerve fibers connecting the left and...
DefinitionX-linked dominant Chondrodysplasia Punctata (CDPX1) is a rare genetic disorder that affects bone and cartilage? development. X-Linked Dominant Chondrodysplasia Punctata (CDPX1) is a genetic condition that...
DefinitionX-linked dominant Coffin-Lowry syndrome is a rare genetic condition that affects how the brain, bones, and other body systems grow and work. It is present from...
DefinitionX-linked dominant congenital? hemidysplasia with ichthyosiform nevus and limb defects is usually called CHILD syndrome. It is a very rare genetic disease present from birth. It...
DefinitionX-Linked Dominant Disorders are a group of genetic conditions that can affect both males and females, but they are often more severe in males. In this...
DefinitionX-linked dominant Xp11.23–p11.22 duplication syndrome (also called Xp11.22–p11.23 duplication / microduplication syndrome) is a rare genetic condition where a copied-extra piece (duplication) on the X-chromosome (region...
