Singleton Merten syndrome
Singleton Merten syndrome noun: an autosomal-dominant genetic disorder with variable expression with an onset of symptoms during childhood.
Noun
Singleton Merten syndrome (uncountable)
- An autosomal-dominant genetic disorder with variable expression with an onset of symptoms during childhood.
Questions about Singleton Merten syndrome
- What does Singleton Merten syndrome mean?
- Singleton Merten syndrome means an autosomal-dominant genetic disorder with variable expression with an onset of symptoms during childhood.
- What part of speech is Singleton Merten syndrome?
- Singleton Merten syndrome is a noun.
Words near Singleton Merten syndrome in the dictionary
Source and license
Adapted from Wiktionary: Singleton Merten 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: “Singleton Merten syndrome.” Word.ws, https://word.ws/singleton_merten_syndrome. Based on Wiktionary, CC BY-SA 4.0.
