Greig cephalopolysyndactyly syndrome (Q3508649)

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acrocephalosyndactylia that has material basis in mutation in the GLI3 gene which results in abnormal development located in limb, located in head, located in face
  • polysyndactyly with peculiars skull shape
  • Polysyndactyly With Peculiar Skull Shape
  • Greig syndrome
  • GREIG CEPHALOPOLYSYNDACTYLY SYNDROME
  • GCPS
  • Greig Cephalosyndactyly Syndrome
  • GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS
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Language Label Description Also known as
English
Greig cephalopolysyndactyly syndrome
acrocephalosyndactylia that has material basis in mutation in the GLI3 gene which results in abnormal development located in limb, located in head, located in face
  • polysyndactyly with peculiars skull shape
  • Polysyndactyly With Peculiar Skull Shape
  • Greig syndrome
  • GREIG CEPHALOPOLYSYNDACTYLY SYNDROME
  • GCPS
  • Greig Cephalosyndactyly Syndrome
  • GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS

Statements

Greig syndrome
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Identifiers

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