PedAM
Pediatric Disease Annotations & Medicines
| Disease | malabsorption syndrome |
| Phenotype | C0002888|megaloblastic anemia |
| Sentences | 3 |
| PubMedID- 24025485 | Mutations in exons 1–4 of the human amnionless gene cause megaloblastic anemia, due to malabsorption of cbl [92]. |
| PubMedID- 26040326 | Imerslund-gräsbeck syndrome (igs) is a rare autosomal recessive disorder characterized by intestinal cobalamin (vitamin b12) malabsorption usually leading to megaloblastic anemia in childhood. |
| PubMedID- 25852856 | Extra-renal manifestations include gi bleeding, megaloblastic anemia due to malabsorption and hepatic rupture [59]. |
Page: 1