| Disease Aliases (21) | Defect of enterocyte intrinsic factor receptor Enterocyte cobalamin malabsorption Enterocyte intrinsic factor receptor, defect of Familial megaloblastic anemia Gräsbeck-imerslund disease Igs Igs1 Igs2 Imerslund-gräsbeck syndrome Megaloblastic anemia, 1 Megaloblastic anemia, finnish type Megaloblastic anemia, norwegian type Mga-1 Mga1 Megaloblastic anemia 1 Pernicious anemia, juvenile, due to selective intestinal malabsorption of vitamin b12, with proteinuria Selective cobalamin malabsorption with proteinuria Juvenile megaloblastic anemia Megaloblastic anemia type 1 Megaloblastic anemia, 1; mga1 |
Associated Genes (2) NCBI-RefSeq: AMN (Amnion associated transmembrane protein) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: CUBN (Cubilin) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Imerslund-Grasbeck syndrome type 1 | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |