Johnson neuroectodermal syndrome

MONDO:0007837

Johnson neuroectodermal syndrome is characterized by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism.

Also known as: Johnson neuroectodermal syndrome, Johnson-McMillin syndrome, alopecia-anosmia-conductive hearing loss-hypogonadism syndrome, alopecia-anosmia-deafness-hypogonadism syndrome, Aadh syndrome, alopecia anosmia deafness hypogonadism syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Johnson neuroectodermal syndrome itself.

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↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ Ectodermal dysplasia syndrome (45)

Including sub-types (0) Tagged with Johnson neuroectodermal syndrome (0)

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