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Disease Mechanism & Classification For Myotonia atrophica (Steinert's disease)

Disease Mechanism & Classification

• Class

  • CLASS/Pediatric disorders (ex)
  • CLASS/Muscle disorder (ex)
  • CLASS/Muscle/tendon/extremities (category)

• Pathophysiology

  • Pathophysiology/Anticipation kindred inheritance earlier onset effect
  • Pathophysiology/Chromosome 19/CTG repeat
  • Pathophysiology/Gene locus chromosome 19
  • Pathophysiology/Gene locus Chromosome 19q
  • Pathophysiology/Gene locus chromosome 3
  • Pathophysiology/Gene Locus Identified/OMIM database
  • Pathophysiology/Genomic base pair repeats mutation
  • Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
  • Pathophysiology/Hereditary anticipation/generations worsen
  • Pathophysiology/Hereditary disease/Adult manifestations
  • Pathophysiology/Hypergonadotrophic hypogonadism
  • Pathophysiology/Secondary Testicular Failure
  • Pathophysiology/Delayed gastric emptying/gastrostasis
  • Pathophysiology/Muscle membrane defect

• Process

  • PROCESS/Atrophic disorders (ex)
  • PROCESS/Autosomal dominant hereditary disease (ex).
  • PROCESS/Hereditary dominance/incomplete penetrance (ex).
  • PROCESS/Hereditofamilial (category)
  • PROCESS/Movement disorder (ex)
  • PROCESS/Variant expressions/Subsets (ex)

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