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This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.
List of results
- WBR0910 + (Classic galactosemia is an autosomal reces … Classic galactosemia is an autosomal recessive disease characterized by the absence of galactose-1-phosphate uridyltransferase (GALT) resulting in the accumulation of galactose-1-phosphate, galactose and galacticol. Although classic galactosemia is associated with cataracts, it is a more severe illness associated with mental retardation, failure to thrive and jaundice.tardation, failure to thrive and jaundice.)