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Results 11 - 20 of 28 for Multiple sclerosis
  1. TSC1 gene 
    ... certain cells. In people with TSC1-related tuberous sclerosis complex, a second TSC1 gene variant typically occurs in multiple cells over an affected person's lifetime. The ...
    https://medlineplus.gov/genetics/gene/tsc1 - Genetics
  2. TSC2 gene 
    ... certain cells. In people with TSC2-related tuberous sclerosis complex, a second TSC2 gene variant typically occurs in multiple cells over an affected person's lifetime. The ...
    https://medlineplus.gov/genetics/gene/tsc2 - Genetics
  3. HBA1 gene 
    ... of this gene leads to the growth of multiple cysts in the kidneys. If the deletion also includes the TSC2 gene, an affected individual will develop tuberous sclerosis complex. This condition is characterized by the growth ...
    https://medlineplus.gov/genetics/gene/hba1 - Genetics
  4. HBA2 gene 
    ... of this gene leads to the growth of multiple cysts in the kidneys. If the deletion also includes the TSC2 gene, an affected individual will develop tuberous sclerosis complex. This condition is characterized by the growth ...
    https://medlineplus.gov/genetics/gene/hba2 - Genetics
  5. Tuberous sclerosis complex 
    ... to form a tumor. In people with tuberous sclerosis complex, a second variant in the TSC1 or TSC2 gene typically occurs in multiple cells over an affected person's lifetime. The ...
    https://medlineplus.gov/.../condition/tuberous-sclerosis-complex - Genetics
  6. VCP gene 
    ... GD, Vesa J, Smith C, Kimonis VE. The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis. J Mol Neurosci. 2011 Nov;45(3):522- ...
    https://medlineplus.gov/genetics/gene/vcp - Genetics
  7. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... GD, Vesa J, Smith C, Kimonis VE. The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis. J Mol Neurosci. 2011 Nov;45(3):522- ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  8. AMER1 gene 
    ... have excessive bone growth (hyperostosis), which leads to multiple ... striata with cranial sclerosis lead to a lack of functional AMER1 protein, ...
    https://medlineplus.gov/genetics/gene/amer1 - Genetics
  9. C9orf72 gene 
    ... hexanucleotide repeat) can occur once or be repeated multiple times in a row; estimates ... amyotrophic lateral sclerosis (ALS), a condition characterized by progressive muscle weakness, ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  10. Systemic scleroderma 
    ... does not have a clear pattern of inheritance. Multiple genetic and environmental factors likely play a part in determining the ... National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/genetics/condition/systemic-scleroderma - Genetics
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