Details of Disease | DrugMAP

General Information of Disease (ID: DISUPNKI)

Disease Name	Maternal riboflavin deficiency
Synonyms	riboflavin deficiency; RBFVD; maternal riboflavin deficiency
Disease Hierarchy	DISBRFME: Disorder of metabolite absorption and transport DISGKSZF: Ariboflavinosis DISUPNKI: Maternal riboflavin deficiency
Disease Identifiers	MONDO ID MONDO_0014013 UMLS CUI C4750953 MedGen ID 1657395 Orphanet ID 411712 SNOMED CT ID 773549000

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DTP Molecule(s)

Gene Name	DTP ID	Evidence Level	Mode of Inheritance	REF
SLC52A1	DT7NOKR	Supportive	Autosomal dominant	[1]
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This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
SLC52A1	OTQ4D276	Supportive	Autosomal dominant	[1]
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References

1	Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency. Mol Genet Metab. 2007 Sep-Oct;92(1-2):109-14. doi: 10.1016/j.ymgme.2007.06.017. Epub 2007 Aug 8.