"vitreoretinochoroidopathy" meaning in All languages combined

{
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      "args": {
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      "expansion": "vitreoretinochoroidopathy (uncountable)",
      "name": "en-noun"
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  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
            "Entries with incorrect language header",
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          "source": "w"
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          "source": "w"
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          "kind": "topical",
          "langcode": "en",
          "name": "Pathology",
          "orig": "en:Pathology",
          "parents": [
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      "examples": [
        {
          "ref": "2016 January 15, “Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing”, in PLOS ONE, →DOI",
          "text": "Additional single cases had final diagnoses of retinitis punctata albescens, autosomal dominant vitreoretinochoroidopathy, atrophy of the choroid and retina resembling gyrate atrophy but without hyperornithinemia, exudative vitreoretinopathy, optic atrophy, Alström syndrome, Bardet Biedl syndrome and Stargardt disease.",
          "type": "quotation"
        }
      ],
      "glosses": [
        "choroidal vitreoretinopathy"
      ],
      "id": "en-vitreoretinochoroidopathy-en-noun-IXKFIDxZ",
      "links": [
        [
          "pathology",
          "pathology"
        ],
        [
          "choroidal",
          "choroidal"
        ],
        [
          "vitreoretinopathy",
          "vitreoretinopathy"
        ]
      ],
      "raw_glosses": [
        "(pathology) choroidal vitreoretinopathy"
      ],
      "tags": [
        "uncountable"
      ],
      "topics": [
        "medicine",
        "pathology",
        "sciences"
      ]
    }
  ],
  "word": "vitreoretinochoroidopathy"
}

{
  "head_templates": [
    {
      "args": {
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      "expansion": "vitreoretinochoroidopathy (uncountable)",
      "name": "en-noun"
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  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
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        "English lemmas",
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      "examples": [
        {
          "ref": "2016 January 15, “Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing”, in PLOS ONE, →DOI",
          "text": "Additional single cases had final diagnoses of retinitis punctata albescens, autosomal dominant vitreoretinochoroidopathy, atrophy of the choroid and retina resembling gyrate atrophy but without hyperornithinemia, exudative vitreoretinopathy, optic atrophy, Alström syndrome, Bardet Biedl syndrome and Stargardt disease.",
          "type": "quotation"
        }
      ],
      "glosses": [
        "choroidal vitreoretinopathy"
      ],
      "links": [
        [
          "pathology",
          "pathology"
        ],
        [
          "choroidal",
          "choroidal"
        ],
        [
          "vitreoretinopathy",
          "vitreoretinopathy"
        ]
      ],
      "raw_glosses": [
        "(pathology) choroidal vitreoretinopathy"
      ],
      "tags": [
        "uncountable"
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      "topics": [
        "medicine",
        "pathology",
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  "word": "vitreoretinochoroidopathy"
}