Disease #05212 (AMDME (ataxia, myoclonia, dysarthria, muscle weakness, exercise intolerance))

Official abbreviation AMDME
Name ataxia, myoclonia, dysarthria, muscle weakness, exercise intolerance
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SLC25A32
Associated tissues brain;skeletal muscle
Disease features severe neuromuscular phenotype
Remarks -
Date created 2016-12-22 09:52:41 +01:00 (CET)
Date last edited N/A


Individuals

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00092292 - - - M yes Netherlands white - - yes Riboflavin AMDME reduced complex II activity in muscle deficiency of mitochondrial FAD-dependent enzymes SLC25A32 - - 1 Debby Hellebrekers
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