Disease Information for Myotonia atrophica (Steinert's disease): Disease Mechanism & Classification

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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/DMPK Gene Mutation
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/ZNF9 Gene Mutation
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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