Congenital defect of folate absorption
| Disease Term | Disease ID | Gene Symbol | Classification | References | Source |
|---|---|---|---|---|---|
| Folate Malabsorption, Hereditary | C0342705 | SLC46A1 | Causal Pathogenic evidence from ClinVar | 11804211, 17129779, 17446347, 18559978, 20686069, 20805364, 21333572, 27604308, 27664775 | ClinVar |
| SARM1 | Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations | - | - |