Orphanet: RFVT2 related riboflavin transporter deficiency
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RFVT2-related riboflavin transporter deficiency

ORPHA:572543

Classification level: Subtype of disorder
  • Synonym(s):
    • RTD2
    • Riboflavin transporter deficiency 2
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Childhood
  • ICD-10: -
  • OMIM: 211530
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -
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