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- ... gene have been identified in people with Pompe disease. Many of these mutations change one of the ... heart problems, and the other features of Pompe disease. More About This Health Condition acid alpha-glucosidase ...
- ... been shown to cause early-onset Alzheimer's disease. Mutations in this gene account for less than ... PSEN2 mutations that cause early-onset Alzheimer's disease change single protein building blocks (amino acids) used ...
- ... variant (also called mutation) that causes Huntington's disease is known as a CAG trinucleotide repeat expansion. ... in the HTT gene. People with Huntington's disease have 36 to more than 120 CAG repeats. ...
- ... than 250 ATP7B gene mutations that cause Wilson disease. About half the mutations change one of the ... ancestry. Approximately one-third of Asians with Wilson disease have a mutation that replaces the amino acid ...
- ... healing and tissue repair. More About This Health Condition MedlinePlus Genetics provides information about Cholangiocarcinoma More About This Health Condition MedlinePlus Genetics provides information about Lung cancer More ...
- ... Lafora progressive myoclonus epilepsy. More About This Health Condition epilepsy, progressive myoclonus type 2, Lafora disease (laforin) epilepsy, progressive myoclonus type 2A, Lafora disease ( ...
- ... Atypical hemolytic-uremic syndrome More About This Health Condition Several mutations in the CFHR5 gene have been found to cause a rare form of kidney disease called C3 glomerulopathy. This disorder damages the kidneys ...
- ... been identified in people with maple syrup urine disease, most often in individuals with mild variants of ... other health problems associated with maple syrup urine disease. More About This Health Condition BCATE2 dihydrolipoamide branched ...
- ... gene have been found to cause Niemann-Pick disease type C2. This type of Niemann-Pick disease is characterized by a buildup of fat within ... to movement problems, neurological impairment, lung and liver disease, and speech and feeding problems. The NPC2 gene ...
- ... the formation of tumors. More About This Health Condition Mutations in the RET gene are the most common genetic cause of Hirschsprung disease, a disorder that causes severe constipation or blockage ...