| Johnson–McMillin syndrome | |
|---|---|
| Other names | Johnson neuroectodermal syndrome, alopecia–anosmia–deafness–hypogonadism syndrome |
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| Johnson–McMillin syndrome is inherited in an autosomal dominant manner. | |
Johnson–McMillin syndrome, also known as Johnson neuroectodermal syndrome, is a neuroectodermal syndrome characterized by conductive hearing loss and alopecia, microtia, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism.