CLRN1, clarin 1, 7401

N. diseases: 77; N. variants: 26
Disease: RETINITIS PIGMENTOSA 61 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3280041
Disease: RETINITIS PIGMENTOSA 61
RETINITIS PIGMENTOSA 61 		0.700 GeneticVariation disease UNIPROT CLRN1 mutations cause nonsyndromic retinitis pigmentosa. 21310491 2011
CUI: C3280041
Disease: RETINITIS PIGMENTOSA 61
RETINITIS PIGMENTOSA 61 		0.700 Biomarker disease GENOMICS_ENGLAND Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family. 9719374 1998
CUI: C3280041
Disease: RETINITIS PIGMENTOSA 61
RETINITIS PIGMENTOSA 61 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C3280041
Disease: RETINITIS PIGMENTOSA 61
RETINITIS PIGMENTOSA 61 		0.700 CausalMutation disease CLINVAR
CUI: C3280041
Disease: RETINITIS PIGMENTOSA 61
RETINITIS PIGMENTOSA 61 		0.700 Biomarker disease CTD_human