Albinism ocular late onset sensorineural deafness: A rare inherited condition characterized by a lack of eye pigmentation and deafness that usually starts in middle-age. Severity of symptoms is variable. More detailed information about the symptoms, causes, and treatments of Albinism ocular late onset sensorineural deafness is available below.
See full list of 8 symptoms of Albinism ocular late onset sensorineural deafness
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Albinism ocular late onset sensorineural deafness is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Albinism ocular late onset sensorineural deafness, or a subtype of Albinism ocular late onset sensorineural deafness,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Albinism ocular late onset sensorineural deafness as a "rare disease".
Source - Orphanet
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