|
MIM:615026 - RIBOFLAVIN DEFICIENCY; RBFVD
Xenbase Genes: slc52a1
Human Disease Resource: MIM
MONDO:0004573 - systemic artery |
MONDO:0014013 - maternal riboflavin deficiency |
|
MONDO:0004573 - systemic artery |
MONDO:0014013 - maternal riboflavin deficiency |