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

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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