Bohring-Opitz syndrome (Q4938225)

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rare genetic syndrome caused by a mutation in the ASXL1 gene
  • BOS
  • BOPS
  • Opitz Trigonocephaly-Like Syndrome
  • Bohring syndrome
  • BOS syndrome
  • Oberklaid-Danks syndrome
  • BOHRING-OPITZ SYNDROME; BOPS
  • C-Like Syndrome
  • BOHRING-OPITZ SYNDROME
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Language Label Description Also known as
English
Bohring-Opitz syndrome
rare genetic syndrome caused by a mutation in the ASXL1 gene
  • BOS
  • BOPS
  • Opitz Trigonocephaly-Like Syndrome
  • Bohring syndrome
  • BOS syndrome
  • Oberklaid-Danks syndrome
  • BOHRING-OPITZ SYNDROME; BOPS
  • C-Like Syndrome
  • BOHRING-OPITZ SYNDROME

Statements

Identifiers

 
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