Johnson-McMillin syndrome
Johnson-McMillin syndrome noun: a neuroectodermal syndrome characterized by alopecia, microtia, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism.
Noun
Johnson-McMillin syndrome (uncountable)
- A neuroectodermal syndrome characterized by alopecia, microtia, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism.
- Synonyms:
- Johnson neuroectodermal syndrome
Synonyms of Johnson-McMillin syndrome
Questions about Johnson-McMillin syndrome
- What does Johnson-McMillin syndrome mean?
- Johnson-McMillin syndrome means a neuroectodermal syndrome characterized by alopecia, microtia, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism.
- What part of speech is Johnson-McMillin syndrome?
- Johnson-McMillin syndrome is a noun.
Words near Johnson-McMillin syndrome in the dictionary
Source and license
Adapted from Wiktionary: Johnson-McMillin 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: “Johnson-McMillin syndrome.” Word.ws, https://word.ws/johnson-mcmillin_syndrome. Based on Wiktionary, CC BY-SA 4.0.
