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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
- WBR0597 + (Classic galactosemia is an autosomal reces … Classic galactosemia is an autosomal recessive disorder characterized by the absence of galactose-1-phosphate uridyltransferase enzyme and subsequent shunting of the galactose metabolism pathway towards the formation of galactitol. Classic galactosemia is associated with development of infantile cataracts, which is unusual among elderly patients., which is unusual among elderly patients.)