Johnson neuroectodermal syndrome (Q83109)
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Johnson neuroectodermal syndrome is characterised by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1480597785 |
||
| English | Johnson neuroectodermal syndrome |
Johnson neuroectodermal syndrome is characterised by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism. |
Statements
CID11:ID_1480597785
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dki-india-ID_1480597785
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Concluído
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13 August 2026
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