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Disease Information for Dystonia musculorum deformans: Disease Mechanism & Classification

Class: CLASS/Neurologic (category)
Pathophysiology: Pathophysiology/Dominant and Autosomal recessive variants; Pathophysiology/Gene alpha-Sarcoglycan LOF mutation; Pathophysiology/Gene locus 1p13; Pathophysiology/Gene locus 1p36; Pathophysiology/Gene locus 7q21; Pathophysiology/Gene locus 8q21; Pathophysiology/gene locus 9q32-q34; Pathophysiology/Gene locus 9q34; Pathophysiology/Gene locus Chromosome 14q; Pathophysiology/Gene locus Chromosome 18; Pathophysiology/Gene locus Chromosome 18p; Pathophysiology/Gene Locus Identified/OMIM database; Pathophysiology/Gene Torsin A abnormal gene; Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/Relative GABA CNS deficiency; Pathophysiology/Sporadic/hereditary/process; Pathophysiology/X-linked and autosomal dominant types
: Pathophysiology/Maternal Chromosome mutation
Process: PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Genetic disorder/Spontaneous mutations/sporadic; PROCESS/Hereditofamilial (category); PROCESS/Movement disorder (ex); PROCESS/Subsets/Variable dominance/sex linkage
: PROCESS/Hyperkinetic Movement disorders

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