Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		0.300 Biomarker GENOMICS_ENGLAND Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice. 31048900

2019
Entrez Id: 745
Gene Symbol: MYRF
MYRF
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		0.300 Biomarker GENOMICS_ENGLAND Autosomal dominant nanophthalmos and high hyperopia associated with a C-terminal frameshift variant in MYRF. 31700225

2019