Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Baller-Gerold syndrome
CUI: C0265308
Disease: Baller-Gerold syndrome
0.700 CausalMutation CLINVAR Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. 12952869 2003
Baller-Gerold syndrome
CUI: C0265308
Disease: Baller-Gerold syndrome
0.700 CausalMutation CLINVAR Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome. 12734318 2003