hypodysfibrinogenemia

noun

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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Meanings

nounhypodysfibrinogenemia (countable and uncountable, plural hypodysfibrinogenemias)

plural hypodysfibrinogenemias

  1. countableuncountableA rare hereditary fibrinogen disorder cause by mutations in one or more of the genes that encode a factor critical for blood clotting, fibrinogen.
Cite this entry
APA

hypodysfibrinogenemia. (n.d.). In WatkinsX Dictionary. Retrieved November 4, 2026, from https://dictionary.watkinsx.com/word/hypodysfibrinogenemia

MLA

“hypodysfibrinogenemia.” WatkinsX Dictionary, https://dictionary.watkinsx.com/word/hypodysfibrinogenemia. Accessed November 4, 2026.

Chicago

WatkinsX Dictionary, s.v. “hypodysfibrinogenemia,” accessed November 4, 2026, https://dictionary.watkinsx.com/word/hypodysfibrinogenemia.

Source: hypodysfibrinogenemia on Wiktionary, CC BY-SA 4.0.