"multiminicore" meaning in All languages combined

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "multi",
        "3": "minicore"
      },
      "expansion": "multi- + minicore",
      "name": "prefix"
    }
  ],
  "etymology_text": "From multi- + minicore.",
  "head_templates": [
    {
      "args": {
        "1": "?"
      },
      "expansion": "multiminicore",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
            "Entries with incorrect language header",
            "Entry maintenance"
          ],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "English terms prefixed with multi-",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with 1 entry",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with entries",
          "parents": [],
          "source": "w"
        }
      ],
      "examples": [
        {
          "ref": "2016 January 21, “Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing”, in PLOS ONE, →DOI:",
          "text": "As in our family, defects in SEPN1 have been associated with a variable clinico-histopathological picture that includes rigid spine muscular dystrophy (RSMD-1), multiminicore disease, desmin-related myopathy with Mallory body-like inclusions (MR-DRM), and also non-specific myopathological features.",
          "type": "quote"
        }
      ],
      "glosses": [
        "multiple minicores"
      ],
      "id": "en-multiminicore-en-noun-FyA9XUGd",
      "links": [
        [
          "multiple",
          "multiple"
        ],
        [
          "minicore",
          "minicore"
        ]
      ]
    }
  ],
  "word": "multiminicore"
}

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "multi",
        "3": "minicore"
      },
      "expansion": "multi- + minicore",
      "name": "prefix"
    }
  ],
  "etymology_text": "From multi- + minicore.",
  "head_templates": [
    {
      "args": {
        "1": "?"
      },
      "expansion": "multiminicore",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        "English countable nouns",
        "English entries with incorrect language header",
        "English lemmas",
        "English nouns",
        "English nouns with unknown or uncertain plurals",
        "English terms prefixed with multi-",
        "English terms with quotations",
        "Pages with 1 entry",
        "Pages with entries"
      ],
      "examples": [
        {
          "ref": "2016 January 21, “Increased Probability of Co-Occurrence of Two Rare Diseases in Consanguineous Families and Resolution of a Complex Phenotype by Next Generation Sequencing”, in PLOS ONE, →DOI:",
          "text": "As in our family, defects in SEPN1 have been associated with a variable clinico-histopathological picture that includes rigid spine muscular dystrophy (RSMD-1), multiminicore disease, desmin-related myopathy with Mallory body-like inclusions (MR-DRM), and also non-specific myopathological features.",
          "type": "quote"
        }
      ],
      "glosses": [
        "multiple minicores"
      ],
      "links": [
        [
          "multiple",
          "multiple"
        ],
        [
          "minicore",
          "minicore"
        ]
      ]
    }
  ],
  "word": "multiminicore"
}