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