(Q1926345)

English

22q13 deletion syndrome

human disease

  • PHELAN-MCDERMID SYNDROME; PHMDS
  • PHMDS
  • Chromosome 22Q13.3 Deletion Syndrome
  • Telomeric 22Q13 Monosomy Syndrome
  • PHELAN-MCDERMID SYNDROME
  • Monosomy type 22q13
  • 22q13 deletion
  • Phelan-McDermid syndrome
  • monosomy 22q13 syndrome
  • 22q13.3 deletion syndrome

Statements

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C157124
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Identifiers

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