Vitamin B 12 Deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A vitamin metabolic disorder that results from low blood levels of vitamin B12. (Human Disease Ontology, DOID_0050731)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D014806
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Genes

2 genes/proteins associated with the disease Vitamin B 12 Deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4 2.88009
CCL2 chemokine (C-C motif) ligand 2 1.165