Apolipoprotein c2 deficiency
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Apolipoprotein C-II Deficiency (disorder) | C1720779 | APOC2 | Causal Pathogenic evidence from ClinVar | 8323539, 24589565, 27297947, 27604308 | ClinVar |
| APOC4-APOC2 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - | ||
| LPL | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - | ||
| Familial apolipoprotein C-II deficiency | 309020, C0268199 | APOC2 | Causal Pathogenic evidence from ClinVar | 24589565 | ClinVar |