MRPS22, mitochondrial ribosomal protein S22, 56945

N. diseases: 78; N. variants: 15
Disease: OVARIAN DYSGENESIS 7 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4748263
Disease: OVARIAN DYSGENESIS 7
OVARIAN DYSGENESIS 7 		0.400 GeneticVariation disease UNIPROT Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency. 29566152 2018
CUI: C4748263
Disease: OVARIAN DYSGENESIS 7
OVARIAN DYSGENESIS 7 		0.400 CausalMutation disease CLINVAR