Mowat-Wilson syndrome
Mowat-Wilson syndrome noun: a rare genetic disorder typically characterized by Hirschsprung's disease, intellectual disability, epilepsy, delayed growth and motor development, congenital heart disease, genitourinary anomalies, and absence of the corpus callosum.
Noun
Mowat-Wilson syndrome (uncountable)
- A rare genetic disorder typically characterized by Hirschsprung's disease, intellectual disability, epilepsy, delayed growth and motor development, congenital heart disease, genitourinary anomalies, and absence of the corpus callosum.
Origin of Mowat-Wilson syndrome
Described by David R. Mowat and Meredith J. Wilson in 1998.
Questions about Mowat-Wilson syndrome
- What does Mowat-Wilson syndrome mean?
- Mowat-Wilson syndrome means a rare genetic disorder typically characterized by Hirschsprung's disease, intellectual disability, epilepsy, delayed growth and motor development, congenital heart disease, genitourinary anomalies, and absence of the corpus callosum.
- What part of speech is Mowat-Wilson syndrome?
- Mowat-Wilson syndrome is a noun.
Words near Mowat-Wilson syndrome in the dictionary
Source and license
Adapted from Wiktionary: Mowat-Wilson 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: “Mowat-Wilson syndrome.” Word.ws, https://word.ws/mowat-wilson_syndrome. Based on Wiktionary, CC BY-SA 4.0.
