Rud syndrome in All languages combined

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{
  "etymology_text": "Named after Einar Rud, who described cases in 1927 and 1929.",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "Rud syndrome (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": "Pages with 1 entry",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with entries",
          "parents": [],
          "source": "w"
        }
      ],
      "glosses": [
        "A poorly characterized disorder, probably of X-linked recessive inheritance, with major manifestations including congenital ichthyosis, hypogonadism, small stature, mental retardation, and epilepsy."
      ],
      "id": "en-Rud_syndrome-en-noun-DSvYds77",
      "links": [
        [
          "congenital",
          "congenital"
        ],
        [
          "ichthyosis",
          "ichthyosis"
        ],
        [
          "hypogonadism",
          "hypogonadism"
        ],
        [
          "epilepsy",
          "epilepsy"
        ]
      ],
      "tags": [
        "uncountable"
      ]
    }
  ],
  "word": "Rud syndrome"
}

[Show JSON for raw wiktextract data ▼] [Hide JSON for raw wiktextract data ▲]

{
  "etymology_text": "Named after Einar Rud, who described cases in 1927 and 1929.",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "Rud syndrome (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",
        "Pages with 1 entry",
        "Pages with entries"
      ],
      "glosses": [
        "A poorly characterized disorder, probably of X-linked recessive inheritance, with major manifestations including congenital ichthyosis, hypogonadism, small stature, mental retardation, and epilepsy."
      ],
      "links": [
        [
          "congenital",
          "congenital"
        ],
        [
          "ichthyosis",
          "ichthyosis"
        ],
        [
          "hypogonadism",
          "hypogonadism"
        ],
        [
          "epilepsy",
          "epilepsy"
        ]
      ],
      "tags": [
        "uncountable"
      ]
    }
  ],
  "word": "Rud syndrome"
}

Download raw JSONL data for Rud syndrome meaning in All languages combined (0.8kB)

This page is a part of the kaikki.org machine-readable All languages combined dictionary. This dictionary is based on structured data extracted on 2026-03-25 from the enwiktionary dump dated 2026-03-03 using wiktextract (05c257f and 9d9a410). The data shown on this site has been post-processed and various details (e.g., extra categories) removed, some information disambiguated, and additional data merged from other sources. See the raw data download page for the unprocessed wiktextract data.

If you use this data in academic research, please cite Tatu Ylonen: Wiktextract: Wiktionary as Machine-Readable Structured Data, Proceedings of the 13th Conference on Language Resources and Evaluation (LREC), pp. 1317-1325, Marseille, 20-25 June 2022. Linking to the relevant page(s) under https://kaikki.org would also be greatly appreciated.

"Rud syndrome" meaning in All languages combined

Noun [English]