Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64131
Gene Symbol: XYLT1
XYLT1 		0.300 GermlineCausalMutation disease ORPHANET "The missing ""link"": an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation." 23982343 2014