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<rdf:Description rdf:about="https://calm.abdn.ac.uk:443/archives/record/catalog/UNIVERSITY%201437/2/1/34" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <dc:title>Slide showing pedigree chart of 'Alkaptonuria'.</dc:title>
  <dc:description>Slide shows black and white pedigree chart of 'Alkaptonuria'.
Title under slide image reads 'Fig. 4 Pedigree of Alkaptonuria, showing consanguinity. Key - [black spot enclosed in square] and [black spot enclosed in circle]= hetrozygous. [Square with diagonal line through] and [circle with diagonal line through] = died in infancy.'
Alkaptonuria is a genetic disease in which the body does not have enough of the homogentisic acid oxidase (HGAO) enzyme.</dc:description>
  <dc:date>Late 19th - early 20th century</dc:date>
</rdf:Description>