Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0.110 GeneticVariation disease BEFREE Common clinical features of XLH include deformities of the lower extremities, short stature, enthesopathies, dental abscesses, as well as skull abnormalities such as craniosynostosis and Chiari I malformation. 31392510 2019
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0.110 Biomarker disease HPO