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Results 1 - 10 of 13 for Amyotrophic lateral sclerosis type 2
  1. Distal myopathy 2 
    ... weakness Matrin 3 distal myopathy MPD2 Myopathia distalis type 2 VCPDM Vocal cord and pharyngeal weakness with distal myopathy Genetic Testing Registry: Amyotrophic lateral sclerosis type 21 Vocal cord and pharyngeal distal myopathy ...
    https://medlineplus.gov/genetics/condition/distal-myopathy-2 - Genetics
  2. SETX gene 
    ... of damaged DNA. MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition At least 125 mutations in the SETX gene have been found to cause ataxia with oculomotor apraxia type 2. This condition is characterized by difficulty coordinating movements ( ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  3. Charcot-Marie-Tooth disease 
    ... can affect the health of the nerve fiber. Type 2 (CMT2) is characterized ... sclerosis (ALS), a condition characterized by progressive muscle weakness, ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  4. Amyotrophic lateral sclerosis 
    ... in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science. 2009 Feb 27;323(5918):1208-1211. doi: 10.1126/science.1165942. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  5. ATXN2 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition ataxin-2 ATX2 ATX2_HUMAN SCA2 Tests of ATXN2 PubMed ...
    https://medlineplus.gov/genetics/gene/atxn2 - Genetics
  6. MATR3 gene 
    ... to the signs and symptoms of distal myopathy 2. More About This Health Condition MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition MATR3_HUMAN matrin- ...
    https://medlineplus.gov/genetics/gene/matr3 - Genetics
  7. DCTN1 gene 
    ... how this mutation causes distal hereditary motor neuronopathy type VIIB. ... amyotrophic lateral sclerosis (ALS). This disorder occurs in mid- to late ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
  8. SOD1 gene 
    ... the protein? Trends Biochem Sci. 2007 Feb;32(2):78-85. doi: 10.1016/j.tibs.2006.12.005. Epub 2007 Jan 5. Citation on PubMed Siddique N, Siddique T. Amyotrophic Lateral Sclerosis Overview. 2001 Mar 23 [updated 2023 Sep 28]. ...
    https://medlineplus.gov/genetics/gene/sod1 - Genetics
  9. CHMP2B gene 
    ... This Health Condition MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition CHM2B_HUMAN CHMP family, member 2B CHMP2.5 chromatin modifying protein 2B DMT1 hVps2-2 vacuolar protein sorting-associated protein 2-2 VPS2 ...
    https://medlineplus.gov/genetics/gene/chmp2b - Genetics
  10. C9orf72 gene 
    ... the C9orf72 gene have been found to cause amyotrophic lateral sclerosis ... ALS. This type of mutation is called a hexanucleotide repeat expansion. ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
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