RPL21, ribosomal protein L21, 6144

N. diseases: 14; N. variants: 1
Disease: Hypotrichosis simplex ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1854310
Disease: Hypotrichosis simplex
Hypotrichosis simplex 		0.310 GeneticVariation disease BEFREE Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex. 21412954 2011
CUI: C1854310
Disease: Hypotrichosis simplex
Hypotrichosis simplex 		0.310 GermlineCausalMutation disease ORPHANET Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex. 21412954 2011