abetalipoproteinemia (Q319812)

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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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Language Label Description Also known as
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

Statements

Abetalipoproteinemia
0 references

Identifiers

MONDO:0008692
 
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