Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 56945
Gene Symbol: MRPS22
MRPS22
CUI: C0949595
Disease: Gonadal Dysgenesis, 46,XX
Gonadal Dysgenesis, 46,XX 		0.300 GermlineCausalMutation ORPHANET Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency. 29566152

2018