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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01277 | Vitamin B12 deficiency anaemia | ... are involved in intestinal absorption and renal tubular reabsorption. Hereditary intrinsic factor deficiency (IFD) is a phenotype that is caused by mutations in CBLIF, the gene encoding intrinsic factor. | Hematologic disease |
(IGS1) CUBN [HSA:8029] [KO:K14616] (IGS2) AMN [HSA:81693] [KO:K18259] (IFD) CBLIF [HSA:2694] [KO:K14615] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |