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Results 1 - 10 of 12 for Amyotrophic lateral sclerosis type 3
  1. Distal myopathy 2 
    ... signs Distal myopathy with vocal cord 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. FUS gene 
    ... in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. ... Nature. 2008 Jul 3;454(7200):126-30. doi: 10.1038/nature06992. ...
    https://medlineplus.gov/genetics/gene/fus - Genetics
  3. Amyotrophic lateral sclerosis 
    ... FRONTOTEMPORAL DEMENTIA; ALS6 AMYOTROPHIC LATERAL SCLEROSIS 7; ALS7 AMYOTROPHIC LATERAL SCLEROSIS 3; ALS3 AMYOTROPHIC LATERAL SCLEROSIS 9; ALS9 AMYOTROPHIC LATERAL ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  4. MATR3 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition MATR3_HUMAN matrin-3 matrin-3 isoform a matrin-3 isoform b ...
    https://medlineplus.gov/genetics/gene/matr3 - Genetics
  5. C9orf72 gene 
    ... Sabatelli M. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. Brain. 2012 Mar;135(Pt 3):784-93. doi: 10.1093/brain/awr366. Citation ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  6. Charcot-Marie-Tooth disease 
    ... the nerve impulse. People with CMT2 may develop amyotrophic lateral sclerosis ... as intermediate type, the nerve impulses are both slowed and reduced ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  7. 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 ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  8. DCTN1 gene 
    ... can be quite long; some are more than 3 feet in length. The dynactin complex is a critical part of a rapid ... sclerosis More About This Health Condition At least five ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
  9. SPG11 gene 
    ... cause the signs and symptoms of spastic paraplegia type 11 by interfering with the protein's ... This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  10. SMN1 gene 
    ... quickly broken down. ... a wide range of severity. There are many types of spinal muscular atrophy that differ in age ...
    https://medlineplus.gov/genetics/gene/smn1 - Genetics
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