"octanoylcarnitine" meaning in All languages combined

{
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      "expansion": "octanoylcarnitine (uncountable)",
      "name": "en-noun"
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  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
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          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
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        {
          "ref": "2015 July 30, Sarah C. Grünert et al., “Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening”, in BMC Medical Genetics, volume 16, →DOI:",
          "text": "In a study with 34 MCAD deficient individuals evaluating the correlation between genotype and biochemical phenotype, patients homozygous for c.985A > G had the highest levels of neonatal octanoylcarnitine followed by compound heterozygotes of c.985A > G and other mutations.",
          "type": "quote"
        }
      ],
      "glosses": [
        "The N-octanoyl derivative of carnitine"
      ],
      "id": "en-octanoylcarnitine-en-noun-QainLwNZ",
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "octanoyl",
          "octanoyl"
        ],
        [
          "carnitine",
          "carnitine"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) The N-octanoyl derivative of carnitine"
      ],
      "tags": [
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
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  ],
  "word": "octanoylcarnitine"
}

{
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  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
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        {
          "ref": "2015 July 30, Sarah C. Grünert et al., “Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening”, in BMC Medical Genetics, volume 16, →DOI:",
          "text": "In a study with 34 MCAD deficient individuals evaluating the correlation between genotype and biochemical phenotype, patients homozygous for c.985A > G had the highest levels of neonatal octanoylcarnitine followed by compound heterozygotes of c.985A > G and other mutations.",
          "type": "quote"
        }
      ],
      "glosses": [
        "The N-octanoyl derivative of carnitine"
      ],
      "links": [
        [
          "organic chemistry",
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      "raw_glosses": [
        "(organic chemistry) The N-octanoyl derivative of carnitine"
      ],
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  "word": "octanoylcarnitine"
}