Disease Information for Gangliosidosis, generalized (GM1): Disease Mechanism & Classification

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Class
CLASS/Jablonski/NIH Archive Anomalies Database
CLASS/Pediatric disorders (ex)
CLASS/Brain/CNS disorder (ex)
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/Adult variant disease milder
Pathophysiology/Def galactocerebroside B-galactosidase
Pathophysiology/Gene locus chromosome 3
Pathophysiology/Gene locus Chromosome 3p
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Subset juvenile form/variant occurs
Pathophysiology/Visceral histiocytosis/foam cells
Pathophysiology/CNS degeneration
Pathophysiology/Developmental degeneration CNS
Pathophysiology/Faulty tubularization long bones
Pathophysiology/Maternal Chromosome mutation
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Lipidosis/storage disorder (ex)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Multiple dysmorphic syndrome (ex)
PROCESS/Sphingolipid metabolic disorder (ex)
PROCESS/Storage disorder (ex)
PROCESS/Two/multiple subsets/disease pattern
PROCESS/Variant expressions/Subsets (ex)
PROCESS/Cerebral lipidoses (ex)
PROCESS/Storage disorder/brain (ex)
PROCESS/Dystostosis/craniofacial (ex)
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