LRP6, LDL receptor related protein 6, 4040

N. diseases: 134; N. variants: 23
Disease: TOOTH AGENESIS, SELECTIVE, 7 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225231
Disease: TOOTH AGENESIS, SELECTIVE, 7
TOOTH AGENESIS, SELECTIVE, 7 		0.600 GeneticVariation disease UNIPROT Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia. 26387593 2015
CUI: C4225231
Disease: TOOTH AGENESIS, SELECTIVE, 7
TOOTH AGENESIS, SELECTIVE, 7 		0.600 Biomarker disease CTD_human
CUI: C4225231
Disease: TOOTH AGENESIS, SELECTIVE, 7
TOOTH AGENESIS, SELECTIVE, 7 		0.600 CausalMutation disease CLINVAR