RPS19, ribosomal protein S19, 6223

N. diseases: 256; N. variants: 17
Disease: Abnormality of radial ray ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray 		0.300 Biomarker phenotype GENOMICS_ENGLAND Autosomal dominant transmission of congenital erythroid hypoplastic anemia with radial abnormalities. 1746615 1991