(Q319812)

Revision as of 13:01, 22 November 2020 by ProteinBoxBot (talk | contribs) (‎Removed claim: instance of (P31): disease (Q12136))
English

abetalipoproteinemia

Human disease

  • familial hypobetalipoproteinemia
  • microsomal triglyceride transfer protein deficiency disease
  • Bassen-Kornzweig Syndrome
  • Microsomal Triglyceride Transfer Protein Deficiency
  • Bassen-Kornzweig disease
  • Homozygous familial hypobetalipoproteinemia
  • Mtp Deficiency
  • ABETALIPOPROTEINEMIA
  • ABL
  • ABETALIPOPROTEINEMIA; ABL
  • Acanthocytosis
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Abetalipoproteinemia
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