UsherKids Australia

Usher syndrome is a genetic condition characterised by hearing loss or deafness, the progressive loss of vision and in some cases, vestibular dysfunction. The loss of vision is caused by an eye disease called Retinitis Pigmentosa (RP), which affects the light-sensitive area of tissue on the back of the eye (the retina). Usher syndrome is a genetic condition characterised by hearing loss or deafness, the progressive loss of vision and in some cases, vestibular dysfunction.

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Usher syndrome is a genetic condition characterised by hearing loss or deafness, the progressive loss of vision and in some cases, vestibular dysfunction. The loss of vision is caused by an eye disease called Retinitis Pigmentosa (RP), which affects the light-sensitive area of tissue on the back of the eye (the retina). Usher syndrome is a genetic condition characterised by hearing loss or deafness, the progressive loss of vision and in some cases, vestibular dysfunction.

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Country (Wikidata; date unspecified)

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Australia

Wikidata Q130302049 property P17. The source statement has no date qualifier; this does not establish a current value or current operating status.

Deterministically projected from an identity-matched Wikidata record. Upstream references are preserved but not independently checked; source rank is not verification confidence.

Rule checked 2026-10-17 · Review due 2027-01-15 · Version 1

Inception (Wikidata)

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2019-08-08

Wikidata Q130302049 property P571. Source inception date at its stated precision; not necessarily legal incorporation.

Deterministically projected from an identity-matched Wikidata record. Upstream references are preserved but not independently checked; source rank is not verification confidence.

Rule checked 2026-10-17 · Review due 2027-01-15 · Version 1

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