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    • LIPID METABOLISM AND TRANSPORT
      • 14    Disorders of lipid metabolism
        • 14.4    Disorders of glycerolipid metabolism
          • Lysophosphatidic acid acyltransferase deficiency
          • Lipin 1 deficiency
          • Lipin 2 deficiency
          • Diacylglycerol acyltransferase deficiency
          • CGI-58 deficiency
          • Adipose triglyceride lipase deficiency
          • Perilipin 1 deficiency
          • Perilipin 4 deficiency
          • Perilipin 5 deficiency
          • Hormone-sensitive lipase deficiency
          • BSCL2-related disease
          • DAGLA-related neuro-ocular syndrome
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  • Pathways
  • Multimers
  • More information
    • About Online IMD
OnlineIMD
  • Home
  • Diseases
    • LIPID METABOLISM AND TRANSPORT
      • 14    Disorders of lipid metabolism
        • 14.4    Disorders of glycerolipid metabolism
          • Lysophosphatidic acid acyltransferase deficiency
          • Lipin 1 deficiency
          • Lipin 2 deficiency
          • Diacylglycerol acyltransferase deficiency
          • CGI-58 deficiency
          • Adipose triglyceride lipase deficiency
          • Perilipin 1 deficiency
          • Perilipin 4 deficiency
          • Perilipin 5 deficiency
          • Hormone-sensitive lipase deficiency
          • BSCL2-related disease
          • DAGLA-related neuro-ocular syndrome
  • Genes
  • Gene products
  • Pathways
  • Multimers
  • More information
    • About Online IMD

Lysophosphatidic acid acyltransferase deficiency

  • Synonym(s)
    • Congenital generalized lipodystrophy type 1, Berardinelli-Seip syndrome
  • Type
    Disease
  • External link(s)
    • IEMbase
  • Gene
    • AGPAT2 / 1-Acylglycerol-3-Phosphate O-Acyltransferase 2
      • 9q34.3
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • 1-Acylglycerol-3-Phosphate O-Acyltransferase 2
  • Disease group(s)
    • 14.4    Disorders of glycerolipid metabolism