Disease: Apolipoprotein C-II Deficiency (disorder) ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Apolipoprotein C-II Deficiency (disorder)
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
0.800 GeneticVariation UNIPROT A missense mutation (Trp 26-->Arg) in exon 3 of the apolipoprotein CII gene in a patient with apolipoprotein CII deficiency (apo CII-Wakayama). 8323539 1993
Apolipoprotein C-II Deficiency (disorder)
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
0.800 CausalMutation CLINVAR