SLC17A5, solute carrier family 17 member 5, 26503

N. diseases: 252; N. variants: 47
Disease: Hydrops Fetalis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		0.400 Biomarker disease GENOMICS_ENGLAND Recurrent nonimmune hydrops fetalis: a rare presentation of sialic acid storage disease. 10546100 1999
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		0.400 Biomarker disease HPO