(Q17144188)

English

Ogden syndrome

X-linked disease resulting from a deficiency in N-terminal acetyltransferase, extreme abrupt behavior, anger issues, characterized by postnatal growth failure with severe delays and dysmorphic features in boys

  • N-alpha-acetyltransferase
  • N-terminal acetyltransferase deficiency
  • OGDNS
  • X-linked Malformation and Infantile Lethality Syndrome
  • OGDEN SYNDROME
  • OGDEN SYNDROME; OGDNS
  • Premature aging appearance-developmental delay-cardiac arrhythmia syndrome

Statements

C188215
0 references

Identifiers

 
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