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Otodental Dysplasia [Supplementary Concept]

Date introduced: November 5, 2012

MeSH Unique ID: C563482

Heading Mapped to:

Entry Terms:

  • Chromosome 11q13 Deletion Syndrome
  • Otodental Syndrome
  • Oculootodental Syndrome
  • Otodental Syndrome With Coloboma

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