"Fabry disease" meaning in All languages combined

{
  "etymology_text": "Named after one of its discoverers, Johannes Fabry (1860–1930).",
  "forms": [
    {
      "form": "Fabry's disease",
      "tags": [
        "alternative"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "Fabry disease (uncountable)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Entries with translation boxes",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with 1 entry",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with entries",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Terms with Finnish translations",
          "parents": [],
          "source": "w"
        }
      ],
      "glosses": [
        "A rare X-linked (inherited) lysosomal storage disease."
      ],
      "id": "en-Fabry_disease-en-noun-dn13-OoC",
      "links": [
        [
          "X-linked",
          "X-linked"
        ],
        [
          "lysosomal",
          "lysosomal"
        ],
        [
          "disease",
          "disease"
        ]
      ],
      "synonyms": [
        {
          "word": "alpha-galactosidase A deficiency"
        },
        {
          "word": "Anderson-Fabry disease"
        },
        {
          "word": "angiokeratoma corporis diffusum"
        }
      ],
      "tags": [
        "uncountable"
      ],
      "translations": [
        {
          "code": "fi",
          "lang": "Finnish",
          "sense": "rare inherited disease",
          "word": "Fabryn tauti"
        }
      ],
      "wikipedia": [
        "Fabry disease"
      ]
    }
  ],
  "word": "Fabry disease"
}

{
  "etymology_text": "Named after one of its discoverers, Johannes Fabry (1860–1930).",
  "forms": [
    {
      "form": "Fabry's disease",
      "tags": [
        "alternative"
      ]
    }
  ],
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "Fabry disease (uncountable)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        "English entries with incorrect language header",
        "English eponyms",
        "English lemmas",
        "English multiword terms",
        "English nouns",
        "English uncountable nouns",
        "Entries with translation boxes",
        "Pages with 1 entry",
        "Pages with entries",
        "Terms with Finnish translations"
      ],
      "glosses": [
        "A rare X-linked (inherited) lysosomal storage disease."
      ],
      "links": [
        [
          "X-linked",
          "X-linked"
        ],
        [
          "lysosomal",
          "lysosomal"
        ],
        [
          "disease",
          "disease"
        ]
      ],
      "tags": [
        "uncountable"
      ],
      "wikipedia": [
        "Fabry disease"
      ]
    }
  ],
  "synonyms": [
    {
      "word": "alpha-galactosidase A deficiency"
    },
    {
      "word": "Anderson-Fabry disease"
    },
    {
      "word": "angiokeratoma corporis diffusum"
    }
  ],
  "translations": [
    {
      "code": "fi",
      "lang": "Finnish",
      "sense": "rare inherited disease",
      "word": "Fabryn tauti"
    }
  ],
  "word": "Fabry disease"
}