Weill-Marchesani syndrome (Q3961695)

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autosomal genetic disease characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities
  • GEMSS syndrome
  • Marchesani-Weill Syndrome
  • Mesodermal Dysmorphodystrophy, Congenital
  • Spherophakia Brachymorphia Syndrome
  • congenital mesodermal dystrophy
  • WMS1
  • Weill-Marchesani Syndrome, Autosomal Recessive
  • WEILL-MARCHESANI SYNDROME 1
  • Weill-Marchesani Syndrome type 1
  • WEILL-MARCHESANI SYNDROME 1; WMS1
  • Spherophakia-Brachymorphia Syndrome
  • Marchesani syndrome
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Language Label Description Also known as
English
Weill-Marchesani syndrome
autosomal genetic disease characterized by short stature, brachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities
  • GEMSS syndrome
  • Marchesani-Weill Syndrome
  • Mesodermal Dysmorphodystrophy, Congenital
  • Spherophakia Brachymorphia Syndrome
  • congenital mesodermal dystrophy
  • WMS1
  • Weill-Marchesani Syndrome, Autosomal Recessive
  • WEILL-MARCHESANI SYNDROME 1
  • Weill-Marchesani Syndrome type 1
  • WEILL-MARCHESANI SYNDROME 1; WMS1
  • Spherophakia-Brachymorphia Syndrome
  • Marchesani syndrome

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Weill–Marchesani syndrome
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