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ENCone-Rod Dystrophy 19 (CORD19)
Alias:
Cord19
Dystrophy, Cone-Rod, Type 19
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Cone-Rod Dystrophy 19, also known as cord19, is related to congenital stationary night blindness and fundus dystrophy. An important gene associated with Cone-Rod Dystrophy 19 is TTLL5 (Tubulin Tyrosine Ligase Like 5). Related phenotypes are reduced visual acuity and undetectable pattern electroretinogram
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MALACARDS
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