Schorderet-Munier-Franceschetti syndrome

noun

A rare genetic oculoauricular syndrome due to mutations in the HMX1 gene.

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Meanings

nounSchorderet-Munier-Franceschetti syndrome (uncountable)
  1. uncountableA rare genetic oculoauricular syndrome due to mutations in the HMX1 gene.
Cite this entry
APA

Schorderet-Munier-Franceschetti syndrome. (n.d.). In WatkinsX Dictionary. Retrieved November 5, 2026, from https://dictionary.watkinsx.com/word/Schorderet-Munier-Franceschetti%20syndrome

MLA

“Schorderet-Munier-Franceschetti syndrome.” WatkinsX Dictionary, https://dictionary.watkinsx.com/word/Schorderet-Munier-Franceschetti%20syndrome. Accessed November 5, 2026.

Chicago

WatkinsX Dictionary, s.v. “Schorderet-Munier-Franceschetti syndrome,” accessed November 5, 2026, https://dictionary.watkinsx.com/word/Schorderet-Munier-Franceschetti%20syndrome.

Source: Schorderet-Munier-Franceschetti syndrome on Wiktionary, CC BY-SA 4.0.