"hypodysfibrinogenemia" meaning in All languages combined

See hypodysfibrinogenemia on Wiktionary

Noun [English]

Forms: hypodysfibrinogenemias [plural]
Head templates: {{en-noun|~}} hypodysfibrinogenemia (countable and uncountable, plural hypodysfibrinogenemias)
  1. A rare hereditary fibrinogen disorder cause by mutations in one or more of the genes that encode a factor critical for blood clotting, fibrinogen. Tags: countable, uncountable
    Sense id: en-hypodysfibrinogenemia-en-noun-lJd1M68I Categories (other): English entries with incorrect language header

Download JSON data for hypodysfibrinogenemia meaning in All languages combined (0.9kB)

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  "lang_code": "en",
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        "A rare hereditary fibrinogen disorder cause by mutations in one or more of the genes that encode a factor critical for blood clotting, fibrinogen."
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      "tags": [
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    }
  ],
  "word": "hypodysfibrinogenemia"
}
{
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        ]
      ],
      "tags": [
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        "uncountable"
      ]
    }
  ],
  "word": "hypodysfibrinogenemia"
}

This page is a part of the kaikki.org machine-readable All languages combined dictionary. This dictionary is based on structured data extracted on 2024-06-04 from the enwiktionary dump dated 2024-05-02 using wiktextract (e9e0a99 and db5a844). 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.