Orphanet: Familial apolipoprotein C II deficiency

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Familial apolipoprotein C-II deficiency


Classification level: Subtype of disorder
  • Synonym(s):
    • Familial APOC2 deficiency
    • Familial apoC-II deficiency
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Childhood, Adolescent
  • ICD-10: E78.3
  • OMIM: 207750
  • UMLS: C0268199  C1720779
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information


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