SSUH2, ssu-2 homolog, 51066

N. diseases: 7; N. variants: 35
Disease: Dentin Dysplasia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011430
Disease: Dentin Dysplasia
Dentin Dysplasia 		0.200 Biomarker disease MGD Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I. 27680507 2017