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Results 1 - 10 of 52 for atrophied
  1. OPA3 gene 
    ... have been found to cause autosomal dominant optic atrophy and cataract. This condition causes slowly worsening vision ... same family. People with this condition have degeneration (atrophy) of the optic nerves, which carry information from ...
    https://medlineplus.gov/genetics/gene/opa3 - Genetics
  2. OAT gene 
    ... gene mutations have been found to cause gyrate atrophy of the choroid and retina (often shortened to gyrate atrophy). These mutations result in a reduced amount of ...
    https://medlineplus.gov/genetics/gene/oat - Genetics
  3. MFN2 gene 
    ... can result in loss of sensation and wasting (atrophy) of muscles in the feet, legs, and hands. ... information from the eyes to the brain (optic atrophy).It is unclear how MFN2 gene mutations lead ...
    https://medlineplus.gov/genetics/gene/mfn2 - Genetics
  4. SMN1 gene 
    ... gene have been found to cause spinal muscular atrophy. This condition is characterized by a loss of motor neurons that leads to weakness and wasting (atrophy) in muscles used for movement (skeletal muscles) that ...
    https://medlineplus.gov/genetics/gene/smn1 - Genetics
  5. SMN2 gene 
    ... the SMN2 gene do not cause spinal muscular atrophy, but they modify the severity of the disorder. ... motor neurons that leads to weakness and wasting (atrophy) in muscles used for movement (skeletal muscles) that ...
    https://medlineplus.gov/genetics/gene/smn2 - Genetics
  6. OPA1 gene 
    ... OPA1 gene have been found to cause optic atrophy type 1. This condition typically results in vision ... of the OPA1 gene mutations that cause optic atrophy type 1 create a premature stop signal in ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
  7. COQ2 gene 
    ... suggested to increase the risk of multiple system atrophy, a progressive brain disorder that affects movement and ... with an increased risk of developing multiple system atrophy in the Japanese population. However, studies have not ...
    https://medlineplus.gov/genetics/gene/coq2 - Genetics
  8. SNCA gene 
    ... found to increase the risk of multiple system atrophy, a progressive brain disorder that affects movement and ... they influence the risk of developing multiple system atrophy. Variations in the SNCA gene appear to affect ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  9. BICD2 gene 
    ... gene have been found to cause spinal muscular atrophy with lower extremity predominance (SMA-LED). This condition is characterized by muscle weakness and wasting (atrophy) in the lower limbs that often begins in ...
    https://medlineplus.gov/genetics/gene/bicd2 - Genetics
  10. TRPV4 gene 
    ... Tooth disease type 2C, congenital distal spinal muscular atrophy, which is characterized by weakness of muscles in the legs and hips, and scapuloperoneal spinal muscular atrophy, which involves weakness and wasting (atrophy) of muscles ...
    https://medlineplus.gov/genetics/gene/trpv4 - Genetics
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