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

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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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