Gene: CLCN7 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1186
Gene Symbol: CLCN7
CLCN7 		0.110 GeneticVariation disease LHGDN ADO caused by mutations in the CLCN7 gene is a frequently symptomatic disease manifested by a high rate of fracture, osteomyelitis, visual loss, and occasional bone marrow failure. 17164308 2007
Entrez Id: 1186
Gene Symbol: CLCN7
CLCN7 		0.110 Biomarker disease HPO