Disease Information for MCAD/Medium chain OH-CoA Dehydrogenase def: Disease Mechanism & Classification

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Class
CLASS/Pediatric disorders (ex)
Pathophysiology
Pathophysiology/ACADM gene locus 1p31
Pathophysiology/Beta oxidation fat defct variant
Pathophysiology/Fails to metabolize fat/mitochondrial level
Pathophysiology/Gene locus Chromosome 1
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Intractable neonatal hypoglycemia
Pathophysiology/Mutation K304E allele
Pathophysiology/Beta-oxidation cycle defect
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Fatty acid Oxidation Disorders (FOD)
PROCESS/Hereditary mitochondrial disorder (ex)
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Esoteric disease (example)
PROCESS/INCIDENCE/Extremely rare disease
PROCESS/Metabolic/storage disorder (category)
PROCESS/Mitochondrial disorders (ex)
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