The genotypes of the diagnosed Danish vHL families with pathogenetic VHL germline mutations include c.278G > A, c.407 T > C, c.433C > T, c.499C > T, c.319C > T, c.353T > C, c.194C > T, c.337C > T, c.520_521ldupAA, c.293A > G, c.269A > T, c.239G > T, c.194C > G, c.481C > T, c.496G > T, c.463 + 1G > T, c.606dupA, c.194C > G, c.548C > A, c.257C > T, c.500G > A, c.191G > C, c.388G > A and others. Here, VHL is linked to von Hippel-Lindau disease.