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Disease Information for Peroneal muscular atrophy(Charcot Mar.): Disease Mechanism & Classification

Class: CLASS/Muscle disorder (ex); CLASS/Muscle/tendon/extremities (category)
: CLASS/Neurologic (category)
Pathophysiology: Pathophysiology/Gene locus 10q21; Pathophysiology/Gene locus 10q21.1-q22.1; Pathophysiology/Gene locus 12p13; Pathophysiology/Gene locus 16p13.3-p12; Pathophysiology/Gene locus 17p11.2; Pathophysiology/Gene locus 17p12-p11; Pathophysiology/Gene locus 1p36; Pathophysiology/Gene locus 1q22; Pathophysiology/Gene locus 21q22; Pathophysiology/Gene locus 3q21; Pathophysiology/Gene locus 8p21; Pathophysiology/Gene locus 9q22; Pathophysiology/Gene locus Chromosome 1; Pathophysiology/Gene locus Chromosome 10; Pathophysiology/Gene locus Chromosome 16; Pathophysiology/Gene locus Chromosome 17; Pathophysiology/Gene locus Chromosome 17p; Pathophysiology/Gene locus chromosome 21; Pathophysiology/Gene locus chromosome 3; Pathophysiology/Gene Locus chromosome 3q; Pathophysiology/Gene locus Chromosome X.; Pathophysiology/Gene Locus Identified/OMIM database; Pathophysiology/Gene locus Xp22.2; Pathophysiology/Gene locus Xq13; Pathophysiology/Gene locus Xq13.1; Pathophysiology/Gene locus Xq26; Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/Hereditary disease/Adult manifestations; Pathophysiology/Sporadic/hereditary/process; Pathophysiology/Variable course subsets/severe/mild
: Pathophysiology/Delayed nerve conduction velocity; Pathophysiology/Demyelination; Pathophysiology/Hereditary Neuropathy
: Pathophysiology/Maternal Chromosome mutation
Process: PROCESS/Atrophic disorders (ex); PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Autosomal recessive disorder (ex); PROCESS/Disease with two subtypes; PROCESS/Genetic disorder/Spontaneous mutations/sporadic; PROCESS/Hereditofamilial (category); PROCESS/Subsets/Variable dominance/sex linkage
: PROCESS/Hereditory motor/sensory neuropathy (ex); PROCESS/Myelin involvement/disorder (ex)

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