CRX, cone-rod homeobox, 1406

N. diseases: 128; N. variants: 28
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0029453
Disease: Osteopenia
Osteopenia
0.010 GeneticVariation disease BEFREE Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene. 11328746 2001