(Q56013735)

English

2p21 microdeletion syndrome

The 2p21 microdeletion syndrome consists of cystinuria, neonatal seizures, hypotonia, severe growthand developmental delay, facial dysmorphism, and lactic acidemia

  • Monosomy 2p21
  • 2p21 deletion syndrome
  • Del(2)(p21)
  • 2p21 deletion

Statements

Identifiers

 
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