| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A vitamin B12 deficiency that is characterized by a lack of vitamin B12 intestinal absorption resulting from a deficiency in the B12 transport protein TCII. (Human Disease Ontology, DOID_0050818) |
| External Link | http://www.omim.org/entry/275350 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the transcobalamin ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TCN2 | transcobalamin II |
