syndromic disease Bonnevie-Ullrich syndrome https://github.com/monarch-initiative/mondo/issues/5089 MONDO:0100492 MEDGEN:315907 UMLS:C1527168 Bonnevie-Ullrich syndrome NCIT:C34434 Bonnevie-Ulrich syndrome A genetic syndrome which occurs in females. It is caused by the inheritance of only one complete X chromosome (45, X). Clinical signs of the symmetrical form are identical to those of Turner syndrome and include bilateral webbing of the neck and edema of the extremities. Clinical characteristics include decreased stature and under-developed sexual organs. Patients usually have a normal life expectancy.