|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease TRANSCOBALAMIN II DEFICIENCY from the curated CTD Gene-Disease Associations dataset.