Schorderet-Munier-Franceschetti syndrome
Schorderet-Munier-Franceschetti syndrome noun: a rare genetic oculoauricular syndrome due to mutations in the HMX1 gene.
Noun
Schorderet-Munier-Franceschetti syndrome (uncountable)
- A rare genetic oculoauricular syndrome due to mutations in the HMX1 gene.
Questions about Schorderet-Munier-Franceschetti syndrome
- What does Schorderet-Munier-Franceschetti syndrome mean?
- Schorderet-Munier-Franceschetti syndrome means a rare genetic oculoauricular syndrome due to mutations in the HMX1 gene.
- What part of speech is Schorderet-Munier-Franceschetti syndrome?
- Schorderet-Munier-Franceschetti syndrome is a noun.
Words near Schorderet-Munier-Franceschetti syndrome in the dictionary
Source and license
Adapted from Wiktionary: Schorderet-Munier-Franceschetti syndrome (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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Cite this entry: “Schorderet-Munier-Franceschetti syndrome.” Word.ws, https://word.ws/schorderet-munier-franceschetti_syndrome. Based on Wiktionary, CC BY-SA 4.0.
