APOC3, apolipoprotein C3, 345

N. diseases: 153; N. variants: 15
Disease: Prader-Willi Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome 		0.010 Biomarker disease BEFREE This is the first report of apoC-III hyposialylation in PWS. 20825553 2010