Prader-Willi syndrome
Prader-Willi syndrome noun: a human disease caused by deletion of part of chromosome 15, and manifested by intellectual disability, a constant feeling of hunger, and other problems.
Noun
Prader–Willi syndrome (uncountable)
- A human disease caused by deletion of part of chromosome 15, and manifested by intellectual disability, a constant feeling of hunger, and other problems.
- Synonyms:
- PWS
Synonyms of Prader-Willi syndrome
Origin of Prader-Willi syndrome
Named after Andrea Prader and Heinrich Willi.
Questions about Prader-Willi syndrome
- What does Prader-Willi syndrome mean?
- Prader-Willi syndrome means a human disease caused by deletion of part of chromosome 15, and manifested by intellectual disability, a constant feeling of hunger, and other problems.
- What part of speech is Prader-Willi syndrome?
- Prader-Willi syndrome is a noun.
Words near Prader-Willi syndrome in the dictionary
Source and license
Adapted from Wiktionary: Prader-Willi 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: “Prader-Willi syndrome.” Word.ws, https://word.ws/prader-willi_syndrome. Based on Wiktionary, CC BY-SA 4.0.
