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Items: 3

1.

Night blindness, congenital stationary [Supplementary Concept]

A clinically and genetically heterogeneous group of nonprogressive retinal disorders that are characterized by impaired NIGHT VISION, decreased VISUAL ACUITY; NYSTAGMUS; MYOPIA, and STRABISMUS. CSNB can be classified into 2 groups based on ELECTRORETINOGRAPHY findings. Germline mutations in several genes have been identified. OMIM: 310500

Date introduced: August 25, 2010

2.

PDE6B protein, human [Supplementary Concept]

RefSeq NM_000283

Date introduced: August 8, 2007

3.

NYX protein, human [Supplementary Concept]

RefSeq NM_022567

Date introduced: December 5, 2000

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