RPL21, ribosomal protein L21, 6144

N. diseases: 14; N. variants: 1
Disease: HYPOTRICHOSIS 12 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4014563
Disease: HYPOTRICHOSIS 12
HYPOTRICHOSIS 12 		0.600 Biomarker disease GENOMICS_ENGLAND Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex. 21412954 2011
CUI: C4014563
Disease: HYPOTRICHOSIS 12
HYPOTRICHOSIS 12 		0.600 GeneticVariation disease UNIPROT Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex. 21412954 2011
CUI: C4014563
Disease: HYPOTRICHOSIS 12
HYPOTRICHOSIS 12 		0.600 CausalMutation disease CLINVAR