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hypodysfibrinogenemia

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.

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.

Forms of hypodysfibrinogenemia

pluralhypodysfibrinogenemias

Questions about hypodysfibrinogenemia

What does hypodysfibrinogenemia mean?
Hypodysfibrinogenemia means a rare hereditary fibrinogen disorder cause by mutations in one or more of the genes that encode a factor critical for blood clotting, fibrinogen.
What part of speech is hypodysfibrinogenemia?
Hypodysfibrinogenemia is a noun.
What is the plural of hypodysfibrinogenemia?
The plural of hypodysfibrinogenemia is hypodysfibrinogenemias.

Words near hypodysfibrinogenemia in the dictionary

  1. hypodopaminergic
  2. hypodopaminergism
  3. hypodorian
  4. hypodynamia
  5. hypodynamic
  6. hypodysfibrinogenemia
  7. hypodysplasia
  8. hypodysplastic
  9. hypoecho
  10. hypoechogenic
  11. hypoechogenicity

Source and license

Adapted from Wiktionary: hypodysfibrinogenemia (page history and authors). Text available under the Creative Commons Attribution-ShareAlike 4.0 license. Word.ws reformatted the entry and added links. Wiktionary data of 2026-09-02.

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