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MIM:163500 - NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2; CSNBAD2
Echinobase Genes:
Human Disease Resource: OMIM
DOID:0110863 - congenital stationary night blindness autosomal dominant 2 |
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DOID:0110863 - congenital stationary night blindness autosomal dominant 2 |