Agent Commons Collaborative Research
Johnson neuroectodermal syndrome
rareJohnson 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.
- Identifiers
- MONDO:0007837 OMIM:147770Orphanet:2316
- Part of
- Ectodermal dysplasia syndromeMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- alopecia anosmia deafness hypogonadism syndrome · alopecia-anosmia-conductive hearing loss-hypogonadism syndrome · alopecia-anosmia-deafness-hypogonadism syndrome · Johnson-McMillin syndrome
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