Disease Information for Hurler's mucopolysaccharidosis syndrome: Disease Mechanism & Classification

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Class
CLASS/Jablonski/NIH Archive Anomalies Database
CLASS/Pediatric disorders (ex)
CLASS/Facial area manifestation/disorder (ex)
CLASS/Skeletal (category)
CLASS/Connective tissue/Mesenchyme matrix disorder
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Lysosome storage disorder (ex)
Pathophysiology/Myocardial Ischemia Non-Arteriosclerosis
Pathophysiology/Demyelination
Pathophysiology/accumulation Heparan and Dermatan Sulfate
Pathophysiology/Accumulation Heparan Sulfate
Pathophysiology/Maternal Chromosome mutation
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Eponymic (category)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Mucopolysaccharidoses (ex)
PROCESS/Multiple dysmorphic syndrome (ex)
PROCESS/Storage disorder (ex)
PROCESS/Storage disorder/brain (ex)
PROCESS/Dwarfism/miscellaneous skeletal dis (ex)
PROCESS/Dystostosis/craniofacial (ex)
PROCESS/Vertebral anomalous congenital syndrome
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