Omenn syndrome
Omenn syndrome noun: an autosomal-recessive severe combined immunodeficiency associated with hypomorphic missense mutations in certain genes.
Noun
Omenn syndrome (uncountable)
- An autosomal-recessive severe combined immunodeficiency associated with hypomorphic missense mutations in certain genes.
Origin of Omenn syndrome
First characterized in 1965 by G. Omenn.
Questions about Omenn syndrome
- What does Omenn syndrome mean?
- Omenn syndrome means an autosomal-recessive severe combined immunodeficiency associated with hypomorphic missense mutations in certain genes.
- What part of speech is Omenn syndrome?
- Omenn syndrome is a noun.
Words near Omenn syndrome in the dictionary
Source and license
Adapted from Wiktionary: Omenn 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.
Last updated:
Cite this entry: “Omenn syndrome.” Word.ws, https://word.ws/omenn_syndrome. Based on Wiktionary, CC BY-SA 4.0.
