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Concept information

disease > genetic disease > hereditary disease > Usher syndrome
... > disease > nervous system diseases > neurological disorder > auditory disorder > hearing loss > Usher syndrome
disease > ENT disease > auditory disorder > hearing loss > Usher syndrome
disease > genetic disease > hereditary disease > retinitis pigmentosa > Usher syndrome
... > disease > eye disease > retinopathy > retinitis > retinitis pigmentosa > Usher syndrome

Terme préférentiel

Usher syndrome  

Définition

  • Usher syndrome, also known as Hallgren syndrome, Usher–Hallgren syndrome, retinitis pigmentosa–dysacusis syndrome or dystrophia retinae dysacusis syndrome, is a rare genetic disorder caused by a mutation in any one of at least 11 genes resulting in a combination of hearing loss and visual impairment. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-W7JQXDDR-W

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