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Summary Literature (0)
OMIM:610445 - NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1

Referenced Disease Ontology:
DOID:0110862 - congenital stationary night blindness autosomal dominant 1

Human Disease Resources: OMIM

Xenbase Genes: rho, rho.2

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Version: 4.11.2


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