WT1, WT1 transcription factor, 7490

N. diseases: 446; N. variants: 61
Disease: Hypergonadotropic Ovarian Failure, X-Linked ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3494522
Disease: Hypergonadotropic Ovarian Failure, X-Linked
Hypergonadotropic Ovarian Failure, X-Linked 		0.300 Biomarker disease CTD_human Novel WT1 Missense Mutations in Han Chinese Women with Premature Ovarian Failure. 26358501 2015