Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020555
Disease: Hypertrichosis
Hypertrichosis
0.110 GeneticVariation disease BEFREE De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. 29100093 2017
CUI: C0020555
Disease: Hypertrichosis
Hypertrichosis
0.110 Biomarker disease HPO