FMOD, fibromodulin, 2331

N. diseases: 54; N. variants: 1
Disease: MYOPIA 3 (disorder) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1864111
Disease: MYOPIA 3 (disorder)
MYOPIA 3 (disorder) 		0.010 GeneticVariation disease BEFREE We screened individuals for lumican and fibromodulin sequence alterations from the original MYP3 family, and from a second high grade myopia pedigree that showed suggestive linkage to both the MYP3 interval and to chromosome 1q32. 15592176 2004