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482306

http://data.parliament.uk/terms/482306

is preferred true more like this
attribute ID more like this
broader
346512
pref label Rare diseases more like this
422827
pref label Chromosome abnormalities more like this
91504
pref label Hereditary diseases more like this
class ID more like this
pref label Fragile X syndrome more like this
is primary topic of 482306.html